A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515586



Internal ID15443197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53635905..53644791hg38UCSC Ensembl
Innerchr19:54139159..54148045hg19UCSC Ensembl
Innerchr19:58830971..58839857hg18UCSC Ensembl
Innerchr19:58830971..58839857hg17UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg388887
hg198887
hg188887
hg178887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664005, nssv685843
Samples
Known GenesDPRX
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515586
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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