A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706068



Internal ID15096034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103139527..103139982hg38UCSC Ensembl
Innerchr9:105901809..105902264hg19UCSC Ensembl
Innerchr9:104941630..104942085hg18UCSC Ensembl
Innerchr9:102981364..102981819hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38456
hg19456
hg18456
hg17456
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516844
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706068
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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