A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661419



Internal ID18959700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55552911..55656825hg38UCSC Ensembl
Innerchr7:55620604..55724518hg19UCSC Ensembl
Innerchr7:55588098..55692012hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38103915
hg19103915
hg18103915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019204
Supporting Variants
Samples
Known GenesVOPP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661419
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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