A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3626511



Internal ID18924792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:59403959..59454303hg38UCSC Ensembl
Innerchr4:60269677..60320021hg19UCSC Ensembl
Innerchr4:59952272..60002616hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3850345
hg1950345
hg1850345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009160
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)nssv3626511
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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