A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579742



Internal ID16367151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42918847..43158934hg38UCSC Ensembl
Innerchr19:43422999..43663086hg19UCSC Ensembl
Innerchr19:48114839..48354926hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38240088
hg19240088
hg18240088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6474n54
Supporting Variantsnssv1149947
SamplesNINDS_156
Known GenesPSG11, PSG2, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579742
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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