A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517310



Internal ID15097917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8779046..8836312hg38UCSC Ensembl
Innerchr3:8820732..8877996hg19UCSC Ensembl
Innerchr3:8795732..8852996hg18UCSC Ensembl
Innerchr3:8795732..8852996hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3857267
hg1957265
hg1857265
hg1757265
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv275n21
Supporting Variantsnssv655041, nssv704536, nssv683194, nssv685880, nssv663971, nssv661175, nssv656362, nssv659075, nssv654706, nssv705314, nssv658936, nssv655693, nssv664676, nssv655174, nssv689381, nssv693415, nssv689464, nssv689073, nssv679440, nssv671024, nssv670322, nssv680675, nssv651679, nssv653002, nssv687914
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517310
Frequency
Sample Size2026
Observed Gain25
Observed Loss0
Observed Complex0
Frequencyn/a


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