A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899915



Internal ID16193871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43380933..43455962hg38UCSC Ensembl
Innerchr19:43885085..43960114hg19UCSC Ensembl
Innerchr19:48576925..48651954hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3875030
hg1975030
hg1875030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579850
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)nssv899915
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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