A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033004



Internal ID19122226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97622914..97683387hg38UCSC Ensembl
Innerchr7:97252226..97312699hg19UCSC Ensembl
Innerchr7:97090162..97150635hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3860474
hg1960474
hg1860474
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655253
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)nsv1033004
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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