A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061584



Internal ID18804115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:45353668..45392721hg38UCSC Ensembl
Innerchr19:45856926..45895979hg19UCSC Ensembl
Innerchr19:50548766..50587819hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3839054
hg1939054
hg1839054
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3606n100
Supporting Variantsnssv3573800
Samples
Known GenesERCC2, PPP1R13L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061584
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