A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv895768



Internal ID16189724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18280264..18281808hg38UCSC Ensembl
Innerchr19:18391074..18392618hg19UCSC Ensembl
Innerchr19:18252074..18253618hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381545
hg191545
hg181545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578751
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)nssv895768
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer