A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579664



Internal ID16367073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42802004..43052691hg38UCSC Ensembl
Innerchr19:43306156..43556843hg19UCSC Ensembl
Innerchr19:47997996..48248683hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38250688
hg19250688
hg18250688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6465n54
Supporting Variantsnssv899661, nssv899658, nssv899656, nssv899660, nssv899659, nssv899657
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579664
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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