A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666231



Internal ID15402883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133255801..133258115hg38UCSC Ensembl
Innerchr9:136131188..136133506hg19UCSC Ensembl
Innerchr9:135121009..135123327hg18UCSC Ensembl
Innerchr9:133160742..133163060hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg382315
hg192319
hg182319
hg172319
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516103
Supporting Variants
Samples
Known GenesABO
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666231
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