A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518287



Internal ID15445580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:61293591..61299246hg38UCSC Ensembl
Innerchr13:61867724..61873379hg19UCSC Ensembl
Innerchr13:60765725..60771380hg18UCSC Ensembl
Innerchr13:60765725..60771380hg17UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg385656
hg195656
hg185656
hg175656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694222
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518287
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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