A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700858



Internal ID15437510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95383629..95395670hg38UCSC Ensembl
Innerchr13:96035883..96047924hg19UCSC Ensembl
Innerchr13:94833884..94845925hg18UCSC Ensembl
Innerchr13:94833884..94845925hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3812042
hg1912042
hg1812042
hg1712042
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524855
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700858
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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