A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616088



Internal ID18914369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:355495..429034hg38UCSC Ensembl
Innerchr4:349284..422823hg19UCSC Ensembl
Innerchr4:339284..412823hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3873540
hg1973540
hg1873540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012409
Supporting Variants
Samples
Known GenesABCA11P, ZNF141
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616088
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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