A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149926



Internal ID15873722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42870449..43158934hg38UCSC Ensembl
Innerchr19:43374601..43663086hg19UCSC Ensembl
Innerchr19:48066441..48354926hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38288486
hg19288486
hg18288486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579724
Supporting Variants
SamplesHGDP00319
Known GenesPSG1, PSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149926
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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