A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3633892



Internal ID18932173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:80132575..80181905hg38UCSC Ensembl
Innerchr4:81053729..81103059hg19UCSC Ensembl
Innerchr4:81272753..81322083hg18UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3849331
hg1949331
hg1849331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003476
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)nssv3633892
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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