A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3738066



Internal ID18689661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35822..66815hg38UCSC Ensembl
Innerchr4:35822..66707hg19UCSC Ensembl
Innerchr4:25822..56707hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3830994
hg1930886
hg1830886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002858
Supporting Variants
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)nssv3738066
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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