A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599642



Internal ID18897923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16583997..16612564hg38UCSC Ensembl
Innerchr20:16564642..16593209hg19UCSC Ensembl
Innerchr20:16512642..16541209hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3828568
hg1928568
hg1828568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057674
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)nssv3599642
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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