A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672645



Internal ID15409297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:46212088..46225538hg38UCSC Ensembl
Innerchr7:46251686..46265136hg19UCSC Ensembl
Innerchr7:46218211..46231661hg18UCSC Ensembl
Innerchr7:46024926..46038376hg17UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3813451
hg1913451
hg1813451
hg1713451
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520026
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672645
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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