A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527418



Internal ID15454711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:46315906..46319846hg38UCSC Ensembl
Innerchr4:46317923..46321863hg19UCSC Ensembl
Innerchr4:46012680..46016620hg18UCSC Ensembl
Innerchr4:46158851..46162791hg17UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg383941
hg193941
hg183941
hg173941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703856
Samples
Known GenesGABRA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527418
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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