A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519037



Internal ID15099644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:53652237..53667339hg38UCSC Ensembl
Innerchr6:53517035..53532137hg19UCSC Ensembl
Innerchr6:53624994..53640096hg18UCSC Ensembl
Innerchr6:53624994..53640096hg17UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3815103
hg1915103
hg1815103
hg1715103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696506
Samples
Known GenesKLHL31
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519037
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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