A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579699



Internal ID16367108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42851743..43240575hg38UCSC Ensembl
Innerchr19:43355895..43744727hg19UCSC Ensembl
Innerchr19:48047735..48436567hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38388833
hg19388833
hg18388833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6467n54
Supporting Variantsnssv899709
Samples
Known GenesLOC284344, PSG1, PSG10P, PSG11, PSG2, PSG4, PSG5, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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