A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519342



Internal ID15446635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43299988..43303548hg38UCSC Ensembl
Innerchr4:43302005..43305565hg19UCSC Ensembl
Innerchr4:42996762..43000322hg18UCSC Ensembl
Innerchr4:43142933..43146493hg17UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg383561
hg193561
hg183561
hg173561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689247, nssv655512, nssv657749, nssv692583
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519342
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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