A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661699



Internal ID18959980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62506780..62951872hg38UCSC Ensembl
Innerchr7:61846306..62412250hg19UCSC Ensembl
Innerchr7:61483741..62049685hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38445093
hg19565945
hg18565945
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030517
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)nssv3661699
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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