A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701867



Internal ID15438519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6965195..6991683hg38UCSC Ensembl
Innerchr11:6986426..7012914hg19UCSC Ensembl
Innerchr11:6943002..6969490hg18UCSC Ensembl
Innerchr11:6943002..6969490hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3826489
hg1926489
hg1826489
hg1726489
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525706
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701867
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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