A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026796



Internal ID19116014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184192620..184216841hg38UCSC Ensembl
Innerchr4:185113773..185137994hg19UCSC Ensembl
Innerchr4:185350767..185374988hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3824222
hg1924222
hg1824222
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744531
Samples
Known GenesENPP6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026796
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