A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517671



Internal ID15444964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:55160422..55160928hg38UCSC Ensembl
Innerchr3:55194450..55194956hg19UCSC Ensembl
Innerchr3:55169490..55169996hg18UCSC Ensembl
Innerchr3:55169490..55169996hg17UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38507
hg19507
hg18507
hg17507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688073, nssv652778
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517671
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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