A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998165



Internal ID18811015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29013..104520hg38UCSC Ensembl
Innerchr4:29013..104407hg19UCSC Ensembl
Innerchr4:19013..94407hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3875508
hg1975395
hg1875395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5063n100
Supporting Variantsnssv3615254
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)nsv998165
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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