A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700721



Internal ID15090687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125388505..125394240hg38UCSC Ensembl
Innerchr9:128150784..128156519hg19UCSC Ensembl
Innerchr9:127190605..127196340hg18UCSC Ensembl
Innerchr9:125230338..125236073hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385736
hg195736
hg185736
hg175736
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515979
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700721
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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