A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525098



Internal ID15452391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:40507202..40509434hg38UCSC Ensembl
Innerchr6:40474941..40477173hg19UCSC Ensembl
Innerchr6:40582919..40585151hg18UCSC Ensembl
Innerchr6:40582919..40585151hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg382233
hg192233
hg182233
hg172233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701157
Samples
Known GenesLRFN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525098
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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