A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639529



Internal ID18937810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133323922..133385035hg38UCSC Ensembl
Innerchr4:134245077..134306190hg19UCSC Ensembl
Innerchr4:134464527..134525640hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3861114
hg1961114
hg1861114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015916
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)nssv3639529
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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