A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697804



Internal ID15434456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:79036372..79037584hg38UCSC Ensembl
Innerchr9:81651288..81652500hg19UCSC Ensembl
Innerchr9:80841108..80842320hg18UCSC Ensembl
Innerchr9:78880842..78882054hg17UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg381213
hg191213
hg181213
hg171213
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521127
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697804
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