A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004013



Internal ID18746544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..71674hg38UCSC Ensembl
Innerchr4:12269..71566hg19UCSC Ensembl
Innerchr4:2269..61566hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3859406
hg1959298
hg1859298
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5056n100
Supporting Variantsnssv3615151, nssv3615150, nssv3615149, nssv3615152, nssv3615153
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004013
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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