A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697803



Internal ID15087769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:73648191..73667097hg38UCSC Ensembl
Innerchr11:73359236..73378142hg19UCSC Ensembl
Innerchr11:73036884..73055790hg18UCSC Ensembl
Innerchr11:73036884..73055790hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3818907
hg1918907
hg1818907
hg1718907
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521125
Supporting Variants
Samples
Known GenesPLEKHB1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697803
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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