A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698215



Internal ID15434867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6142157..6291125hg38UCSC Ensembl
Innerchr9:6142157..6291125hg19UCSC Ensembl
Innerchr9:6132157..6281125hg18UCSC Ensembl
Innerchr9:6132157..6281125hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38148969
hg19148969
hg18148969
hg17148969
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521598
Supporting Variants
Samples
Known GenesIL33
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698215
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