A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899683



Internal ID16193639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42813916..43174544hg38UCSC Ensembl
Innerchr19:43318068..43678696hg19UCSC Ensembl
Innerchr19:48009908..48370536hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38360629
hg19360629
hg18360629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579679
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG2, PSG5, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899683
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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