A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701157



Internal ID15437809
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525098
Supporting Variants
Samples
Known GenesLRFN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701157
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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