A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616188



Internal ID18567783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8223942..8423104hg38UCSC Ensembl
Innerchr4:8225669..8424831hg19UCSC Ensembl
Innerchr4:8276569..8475731hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38199163
hg19199163
hg18199163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009011
Supporting Variants
Samples
Known GenesACOX3, HTRA3, SH3TC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616188
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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