A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517123



Internal ID15444416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14805759..14808898hg38UCSC Ensembl
Innerchr19:14916571..14919710hg19UCSC Ensembl
Innerchr19:14777571..14780710hg18UCSC Ensembl
Innerchr19:14777571..14780710hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383140
hg193140
hg183140
hg173140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661713, nssv677090, nssv653822, nssv679045, nssv679587, nssv658069, nssv692122, nssv666784
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517123
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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