A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696003



Internal ID15432655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:140625525..140626845hg38UCSC Ensembl
Innerchr5:140005110..140006430hg19UCSC Ensembl
Innerchr5:139985294..139986614hg18UCSC Ensembl
Innerchr5:139985294..139986614hg17UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg381321
hg191321
hg181321
hg171321
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518560
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696003
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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