A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516403



Internal ID15443696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15204641..15206508hg38UCSC Ensembl
Innerchr11:15226187..15228054hg19UCSC Ensembl
Innerchr11:15182763..15184630hg18UCSC Ensembl
Innerchr11:15182763..15184630hg17UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381868
hg191868
hg181868
hg171868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673302, nssv654987, nssv668096, nssv702965, nssv688651
Samples
Known GenesINSC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516403
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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