A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655626



Internal ID18953907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65949077..65992450hg38UCSC Ensembl
Innerchr7:65414064..65457437hg19UCSC Ensembl
Innerchr7:65051499..65094872hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3843374
hg1943374
hg1843374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028971
Supporting Variants
Samples
Known GenesGUSB, VKORC1L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655626
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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