A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699844



Internal ID15436496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131842271..131843615hg38UCSC Ensembl
Innerchr9:134717658..134719002hg19UCSC Ensembl
Innerchr9:133707479..133708823hg18UCSC Ensembl
Innerchr9:131747212..131748556hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381345
hg191345
hg181345
hg171345
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523988
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699844
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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