A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524318



Internal ID15451611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:64954203..64960865hg38UCSC Ensembl
Innerchr13:65528335..65534997hg19UCSC Ensembl
Innerchr13:64426336..64432998hg18UCSC Ensembl
Innerchr13:64426336..64432998hg17UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg386663
hg196663
hg186663
hg176663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700221
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524318
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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