A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899916



Internal ID16193872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43416460..43450962hg38UCSC Ensembl
Innerchr19:43920612..43955114hg19UCSC Ensembl
Innerchr19:48612452..48646954hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3834503
hg1934503
hg1834503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579851
Supporting Variants
Samples
Known GenesTEX101
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899916
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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