A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1002765



Internal ID15950035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86300674..86967515hg38UCSC Ensembl
Innerchr4:87221827..87888667hg19UCSC Ensembl
Innerchr4:87440851..88107691hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38666842
hg19666841
hg18666841
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594787
Supporting Variants
Samples
Known GenesAFF1, C4orf36, LOC100506746, MAPK10, PTPN13, SLC10A6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1002765
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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