A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703824



Internal ID15440476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13380508..13388039hg38UCSC Ensembl
Innerchr9:13380507..13388038hg19UCSC Ensembl
Innerchr9:13370507..13378038hg18UCSC Ensembl
Innerchr9:13370507..13378038hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg387532
hg197532
hg187532
hg177532
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527389
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703824
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer