A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060763



Internal ID18803294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29964373..29987524hg38UCSC Ensembl
Innerchr19:30455280..30478431hg19UCSC Ensembl
Innerchr19:35147120..35170271hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3823152
hg1923152
hg1823152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3511n100
Supporting Variantsnssv3566544, nssv3566543
Samples
Known GenesURI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060763
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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