A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012102



Internal ID18754638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66815..143160hg38UCSC Ensembl
Innerchr4:66707..136942hg19UCSC Ensembl
Innerchr4:56707..126942hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3876346
hg1970236
hg1870236
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5071n100
Supporting Variantsnssv3616032
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)nsv1012102
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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