A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520523



Internal ID15101130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:142100008..142391976hg38UCSC Ensembl
Innerchr3:141818850..142110818hg19UCSC Ensembl
Innerchr3:143301540..143593508hg18UCSC Ensembl
Innerchr3:143301548..143593516hg17UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38291969
hg19291969
hg18291969
hg17291969
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv299n21
Supporting Variantsnssv683522, nssv679761, nssv673753, nssv672004
Samples
Known GenesGK5, TFDP2, XRN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520523
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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