A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698758



Internal ID15435410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:41295438..41302863hg38UCSC Ensembl
Innerchr11:41316988..41324413hg19UCSC Ensembl
Innerchr11:41273564..41280989hg18UCSC Ensembl
Innerchr11:41273564..41280989hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg387426
hg197426
hg187426
hg177426
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523070
Supporting Variants
Samples
Known GenesLRRC4C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698758
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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