A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899697



Internal ID16193653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42817913..43206299hg38UCSC Ensembl
Innerchr19:43322065..43710451hg19UCSC Ensembl
Innerchr19:48013905..48402291hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38388387
hg19388387
hg18388387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579689
Supporting Variants
Samples
Known GenesLOC100289650, 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)nssv899697
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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