A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899798



Internal ID16193754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42960729..43254431hg38UCSC Ensembl
Innerchr19:43464881..43758583hg19UCSC Ensembl
Innerchr19:48156721..48450423hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38293703
hg19293703
hg18293703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579759
Supporting Variants
Samples
Known GenesLOC284344, PSG11, PSG2, PSG4, PSG5, PSG9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899798
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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