A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516720



Internal ID15444013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116336585..116373151hg38UCSC Ensembl
Innerchr11:116207302..116243868hg19UCSC Ensembl
Innerchr11:115712512..115749078hg18UCSC Ensembl
Innerchr11:115712512..115749078hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3836567
hg1936567
hg1836567
hg1736567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv670434, nssv693527
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516720
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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