A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010661



Internal ID18753193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..166232hg38UCSC Ensembl
Innerchr4:12269..160021hg19UCSC Ensembl
Innerchr4:2269..150021hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38153964
hg19147753
hg18147753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5060n100
Supporting Variantsnssv3615219
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)nsv1010661
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