A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655294



Internal ID18953575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97791325..97823215hg38UCSC Ensembl
Innerchr7:97420637..97452527hg19UCSC Ensembl
Innerchr7:97258573..97290463hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3831891
hg1931891
hg1831891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017573
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)nssv3655294
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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