A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023927



Internal ID18766460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:153241280..153829191hg38UCSC Ensembl
Innerchr7:152938365..153526276hg19UCSC Ensembl
Innerchr7:152569298..153157209hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38587912
hg19587912
hg18587912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6761n100
Supporting Variantsnssv3757733, nssv3757732
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)nsv1023927
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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