A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700139



Internal ID15436791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:28935726..28940469hg38UCSC Ensembl
Innerchr7:28975343..28980086hg19UCSC Ensembl
Innerchr7:28941868..28946611hg18UCSC Ensembl
Innerchr7:28748583..28753326hg17UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg384744
hg194744
hg184744
hg174744
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524247
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700139
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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