A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578747



Internal ID16366156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18280260..18281832hg38UCSC Ensembl
Innerchr19:18391070..18392642hg19UCSC Ensembl
Innerchr19:18252070..18253642hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381573
hg191573
hg181573
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6293n54
Supporting Variantsnssv895739, nssv895740, nssv895746, nssv895741, nssv895747, nssv895744, nssv895743, nssv895745, nssv895742, nssv895748
Samples
Known GenesJUND
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578747
Frequency
Sample Size17421
Observed Gain8
Observed Loss2
Observed Complex0
Frequencyn/a


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