A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584778



Internal ID18883059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:39727516..39771320hg38UCSC Ensembl
Innerchr20:38356158..38399962hg19UCSC Ensembl
Innerchr20:37789572..37833376hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3843805
hg1943805
hg1843805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060187
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)nssv3584778
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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