A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696028



Internal ID15432680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:19971251..19997212hg38UCSC Ensembl
Innerchr11:19992797..20018758hg19UCSC Ensembl
Innerchr11:19949373..19975334hg18UCSC Ensembl
Innerchr11:19949373..19975334hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3825962
hg1925962
hg1825962
hg1725962
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518583
Supporting Variants
Samples
Known GenesNAV2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696028
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