A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584835



Internal ID18536430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45257396..45314077hg38UCSC Ensembl
Innerchr20:43886037..43942717hg19UCSC Ensembl
Innerchr20:43319451..43376131hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3856682
hg1956681
hg1856681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056815
Supporting Variants
Samples
Known GenesMATN4, RBPJL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584835
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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