A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564613



Internal ID18516208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6270389..6299325hg38UCSC Ensembl
Innerchr19:6270400..6299336hg19UCSC Ensembl
Innerchr19:6221400..6250336hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3828937
hg1928937
hg1828937
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059525
Supporting Variants
Samples
Known GenesMLLT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564613
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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