A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437746



Internal ID15383052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65207571..65226921hg38UCSC Ensembl
Outerchr3:65200563..65230129hg38UCSC Ensembl
Innerchr3:65193246..65212596hg19UCSC Ensembl
Outerchr3:65186238..65215804hg19UCSC Ensembl
Innerchr3:65168286..65187636hg18UCSC Ensembl
Outerchr3:65161278..65190844hg18UCSC Ensembl
Innerchr3:65150584..65169934hg16UCSC Ensembl
Outerchr3:65143576..65173142hg16UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3829567
hg1929567
hg1829567
hg1629567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv73n17
Supporting Variantsnssv467627
SamplesNA10835
Known Genes
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)nsv437746
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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