A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605705



Internal ID16046428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:947983..1211575hg38UCSC Ensembl
Innerchr7:987619..1251211hg19UCSC Ensembl
Innerchr7:954145..1217737hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38263593
hg19263593
hg18263593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155844
Samples1780862275_A
Known GenesADAP1, C7orf50, COX19, CYP2W1, GPER1, GPR146, MIR339, ZFAND2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605705
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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