A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662191



Internal ID18613786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131334233..131555085hg38UCSC Ensembl
Innerchr7:131018992..131239844hg19UCSC Ensembl
Innerchr7:130669532..130890384hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38220853
hg19220853
hg18220853
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027676
Supporting Variants
Samples
Known GenesMKLN1, PODXL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662191
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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