A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019204



Internal ID19108422
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 StatusM
Merged Variants
Supporting Variantsnssv3661420, nssv3661419
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)nsv1019204
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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