A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061784



Internal ID19151003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8687281..8717236hg38UCSC Ensembl
Innerchr19:8797532..8827581hg19UCSC Ensembl
Innerchr19:8658532..8688581hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3829956
hg1930050
hg1830050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3426n100
Supporting Variantsnssv3564678
Samples
Known GenesACTL9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061784
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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