A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014303



Internal ID18756837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:22869..66815hg38UCSC Ensembl
Innerchr4:22869..66707hg19UCSC Ensembl
Innerchr4:12869..56707hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3843947
hg1943839
hg1843839
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5055n100
Supporting Variantsnssv3615242, nssv3615241
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)nsv1014303
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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