A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3542789



Internal ID18841070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19931704..19954541hg38UCSC Ensembl
Innerchr16:19943026..19965863hg19UCSC Ensembl
Innerchr16:19850527..19873364hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3822838
hg1922838
hg1822838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052157
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)nssv3542789
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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