A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007526



Internal ID18750057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65773..117100hg38UCSC Ensembl
Innerchr4:65665..116981hg19UCSC Ensembl
Innerchr4:55665..106981hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3851328
hg1951317
hg1851317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5069n100
Supporting Variantsnssv3615285, nssv3615284
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)nsv1007526
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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