A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702022



Internal ID15438674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:11303486..11326932hg38UCSC Ensembl
Innerchr4:11305110..11328556hg19UCSC Ensembl
Innerchr4:10914208..10937654hg18UCSC Ensembl
Innerchr4:10981379..11004825hg17UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3823447
hg1923447
hg1823447
hg1723447
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525832
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702022
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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