A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010553



Internal ID18753084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:22869..165271hg38UCSC Ensembl
Innerchr4:22869..159061hg19UCSC Ensembl
Innerchr4:12869..149061hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38142403
hg19136193
hg18136193
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5060n100
Supporting Variantsnssv3615243
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)nsv1010553
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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