A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv898768



Internal ID15846038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35268140..35269510hg38UCSC Ensembl
Innerchr19:35759043..35760413hg19UCSC Ensembl
Innerchr19:40450883..40452253hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381371
hg191371
hg181371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579389
Supporting Variants
Samples
Known GenesUSF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv898768
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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