A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579684



Internal ID16367093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42813916..43290434hg38UCSC Ensembl
Innerchr19:43318068..43794586hg19UCSC Ensembl
Innerchr19:48009908..48486426hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38476519
hg19476519
hg18476519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6471n54
Supporting Variantsnssv899693
Samples
Known GenesLOC100289650, LOC284344, PSG1, PSG10P, PSG11, PSG2, PSG4, PSG5, PSG6, PSG7, PSG9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579684
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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