A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616071



Internal ID18567666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:141044..256048hg38UCSC Ensembl
Innerchr4:134825..249837hg19UCSC Ensembl
Innerchr4:124825..239837hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38115005
hg19115013
hg18115013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001793
Supporting Variants
Samples
Known GenesZNF718, ZNF876P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616071
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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