A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519354



Internal ID15446647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:139900227..139902682hg38UCSC Ensembl
Innerchr3:139619069..139621524hg19UCSC Ensembl
Innerchr3:141101759..141104214hg18UCSC Ensembl
Innerchr3:141101767..141104222hg17UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg382456
hg192456
hg182456
hg172456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692405, nssv693858, nssv655610, nssv701440, nssv674986
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519354
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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