A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704139



Internal ID15440791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50230418..50238989hg38UCSC Ensembl
Innerchr7:50270014..50278585hg19UCSC Ensembl
Innerchr7:50240560..50249131hg18UCSC Ensembl
Innerchr7:50047275..50055846hg17UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg388572
hg198572
hg188572
hg178572
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520090
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704139
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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