A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584724



Internal ID18883005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:30185664..30400778hg38UCSC Ensembl
Innerchr20:29420340..29635454hg19UCSC Ensembl
Innerchr20:28034001..28249115hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg38215115
hg19215115
hg18215115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062766
Supporting Variants
Samples
Known GenesFRG1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584724
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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