A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437166



Internal ID15382472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66938836..66953112hg38UCSC Ensembl
Outerchr13:66925147..66954441hg38UCSC Ensembl
Innerchr13:67512968..67527244hg19UCSC Ensembl
Outerchr13:67499279..67528573hg19UCSC Ensembl
Innerchr13:66410969..66425245hg18UCSC Ensembl
Outerchr13:66397280..66426574hg18UCSC Ensembl
Innerchr13:65310969..65325245hg16UCSC Ensembl
Outerchr13:65297280..65326574hg16UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3829295
hg1929295
hg1829295
hg1629295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467047
SamplesNA10857
Known GenesPCDH9
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nsv437166
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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