A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031117



Internal ID19120338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:46889719..46950187hg38UCSC Ensembl
Innerchr7:46929317..46989785hg19UCSC Ensembl
Innerchr7:46895842..46956310hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3860469
hg1960469
hg1860469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6342n100
Supporting Variantsnssv3661233, nssv3661234
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)nsv1031117
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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