A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517711



Internal ID15445004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112452175..112455417hg38UCSC Ensembl
Innerchr13:113106489..113109731hg19UCSC Ensembl
Innerchr13:112154490..112157732hg18UCSC Ensembl
Innerchr13:112154490..112157732hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg383243
hg193243
hg183243
hg173243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652925, nssv693281
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517711
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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