A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579377



Internal ID16366786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35171354..35182340hg38UCSC Ensembl
Innerchr19:35662257..35673243hg19UCSC Ensembl
Innerchr19:40354097..40365083hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3810987
hg1910987
hg1810987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898724
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579377
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