A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437716



Internal ID15036448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34927280..34927329hg38UCSC Ensembl
Outerchr11:34927039..34928649hg38UCSC Ensembl
Innerchr11:34948827..34948876hg19UCSC Ensembl
Outerchr11:34948586..34950196hg19UCSC Ensembl
Innerchr11:34905403..34905452hg18UCSC Ensembl
Outerchr11:34905162..34906772hg18UCSC Ensembl
Innerchr11:34913136..34913185hg16UCSC Ensembl
Outerchr11:34912895..34914505hg16UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381611
hg191611
hg181611
hg161611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467597
SamplesNA18506
Known GenesPDHX
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)nsv437716
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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