A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662124



Internal ID18960405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122203647..122293112hg38UCSC Ensembl
Innerchr7:121843701..121933166hg19UCSC Ensembl
Innerchr7:121630937..121720402hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3889466
hg1989466
hg1889466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034945
Supporting Variants
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)nssv3662124
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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