A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv894915



Internal ID16188871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14934418..14936823hg38UCSC Ensembl
Innerchr19:15045230..15047635hg19UCSC Ensembl
Innerchr19:14906230..14908635hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382406
hg192406
hg182406
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578685
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv894915
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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