A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057937



Internal ID19147156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27286466..27578429hg38UCSC Ensembl
Innerchr19:27777374..28069337hg19UCSC Ensembl
Innerchr19:32469214..32761177hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38291964
hg19291964
hg18291964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3502n100
Supporting Variantsnssv3572045
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057937
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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