A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517101



Internal ID15444394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153748053..153754374hg38UCSC Ensembl
Innerchr3:153465842..153472163hg19UCSC Ensembl
Innerchr3:154948532..154954853hg18UCSC Ensembl
Innerchr3:154948540..154954861hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg386322
hg196322
hg186322
hg176322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656149, nssv661446, nssv688207, nssv690017, nssv653789
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517101
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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