A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899774



Internal ID16193730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42897784..43187166hg38UCSC Ensembl
Innerchr19:43401936..43691318hg19UCSC Ensembl
Innerchr19:48093776..48383158hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38289383
hg19289383
hg18289383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579736
Supporting Variants
Samples
Known GenesPSG11, PSG2, PSG5, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899774
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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