A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579759



Internal ID16367168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42960729..43254431hg38UCSC Ensembl
Innerchr19:43464881..43758583hg19UCSC Ensembl
Innerchr19:48156721..48450423hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38293703
hg19293703
hg18293703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899798
Samples
Known GenesLOC284344, PSG11, PSG2, PSG4, PSG5, PSG9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579759
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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