A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685843



Internal ID15422495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53635905..53644432hg38UCSC Ensembl
Innerchr19:54139159..54147686hg19UCSC Ensembl
Innerchr19:58830971..58839498hg18UCSC Ensembl
Innerchr19:58830971..58839498hg17UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg388528
hg198528
hg188528
hg178528
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515586
Supporting Variants
Samples
Known GenesDPRX
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685843
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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