A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031176



Internal ID19120397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:63654509..63841733hg38UCSC Ensembl
Innerchr7:63114887..63302111hg19UCSC Ensembl
Innerchr7:62752322..62939546hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38187225
hg19187225
hg18187225
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6433n100
Supporting Variantsnssv3661967
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031176
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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