A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523937



Internal ID15451230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:134796579..134854535hg38UCSC Ensembl
Innerchr5:134132269..134190225hg19UCSC Ensembl
Innerchr5:134160168..134218124hg18UCSC Ensembl
Innerchr5:134160168..134218124hg17UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3857957
hg1957957
hg1857957
hg1757957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699783
Samples
Known GenesC5orf24, DDX46
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523937
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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