A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606276



Internal ID16393685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13788474..13829288hg38UCSC Ensembl
Innerchr7:13828099..13868913hg19UCSC Ensembl
Innerchr7:13794624..13835438hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3840815
hg1940815
hg1840815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155300
SamplesHGDP00942
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606276
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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