A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704684



Internal ID15441336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113641805..113643096hg38UCSC Ensembl
Innerchr9:116404085..116405376hg19UCSC Ensembl
Innerchr9:115443906..115445197hg18UCSC Ensembl
Innerchr9:113483639..113484930hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381292
hg191292
hg181292
hg171292
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516235
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704684
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