A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063883



Internal ID19153102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:55012576..55044452hg38UCSC Ensembl
Innerchr19:55523944..55555820hg19UCSC Ensembl
Innerchr19:60215756..60247632hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3831877
hg1931877
hg1831877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570426
Samples
Known GenesGP6, RDH13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063883
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