A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608376



Internal ID16395785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:126817725..126931023hg38UCSC Ensembl
Innerchr7:126457779..126571077hg19UCSC Ensembl
Innerchr7:126245015..126358313hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38113299
hg19113299
hg18113299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1094253
Samples
Known GenesGRM8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608376
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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