A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3630227



Internal ID18928508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68725894..68802278hg38UCSC Ensembl
Innerchr4:69591612..69667996hg19UCSC Ensembl
Innerchr4:69626201..69702585hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3876385
hg1976385
hg1876385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013885
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)nssv3630227
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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