A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698397



Internal ID15435049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7927803..7929122hg38UCSC Ensembl
Innerchr11:7949350..7950669hg19UCSC Ensembl
Innerchr11:7905926..7907245hg18UCSC Ensembl
Innerchr11:7905926..7907245hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381320
hg191320
hg181320
hg171320
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522758
Supporting Variants
Samples
Known GenesOR10A6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698397
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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