A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3743109



Internal ID19041390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133274617..133377744hg38UCSC Ensembl
Innerchr4:134195772..134298899hg19UCSC Ensembl
Innerchr4:134415222..134518349hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38103128
hg19103128
hg18103128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019048
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3743109
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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