A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv895765



Internal ID16189721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18280260..18282063hg38UCSC Ensembl
Innerchr19:18391070..18392873hg19UCSC Ensembl
Innerchr19:18252070..18253873hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381804
hg191804
hg181804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578749
Supporting Variants
Samples
Known GenesJUND
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv895765
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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