A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv898579



Internal ID15845849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34481093..34482043hg38UCSC Ensembl
Innerchr19:34971998..34972948hg19UCSC Ensembl
Innerchr19:39663838..39664788hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38951
hg19951
hg18951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579349
Supporting Variants
Samples
Known GenesWTIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv898579
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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