A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705686



Internal ID15095652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:36689261..36692010hg38UCSC Ensembl
Innerchr5:36689363..36692112hg19UCSC Ensembl
Innerchr5:36725120..36727869hg18UCSC Ensembl
Innerchr5:36725120..36727869hg17UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg382750
hg192750
hg182750
hg172750
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528986
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705686
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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