A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699852



Internal ID15089818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103201942..103203381hg38UCSC Ensembl
Innerchr9:105964224..105965663hg19UCSC Ensembl
Innerchr9:105004045..105005484hg18UCSC Ensembl
Innerchr9:103043779..103045218hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381440
hg191440
hg181440
hg171440
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)nssv699852
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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