A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003866



Internal ID18746397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..85909hg38UCSC Ensembl
Innerchr4:12269..85800hg19UCSC Ensembl
Innerchr4:2269..75800hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3873641
hg1973532
hg1873532
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5057n100
Supporting Variantsnssv3615189, nssv3615190, nssv3738043
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)nsv1003866
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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