A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517500



Internal ID15444793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:57959419..57977219hg38UCSC Ensembl
Innerchr13:58533553..58551353hg19UCSC Ensembl
Innerchr13:57431554..57449354hg18UCSC Ensembl
Innerchr13:57431554..57449354hg17UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3817801
hg1917801
hg1817801
hg1717801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658122, nssv689936, nssv652196, nssv667360, nssv682572, nssv686861, nssv667992, nssv662730, nssv677422, nssv662316, nssv688787
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517500
Frequency
Sample Size2026
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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