A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696874



Internal ID15433526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64778919..64817515hg38UCSC Ensembl
Innerchr11:64546391..64584987hg19UCSC Ensembl
Innerchr11:64302967..64341563hg18UCSC Ensembl
Innerchr11:64302967..64341563hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3838597
hg1938597
hg1838597
hg1738597
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519478
Supporting Variants
Samples
Known GenesMAP4K2, MEN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696874
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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