A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3719027



Internal ID19017308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:71406816..71454868hg38UCSC Ensembl
Innerchr16:71440719..71488771hg19UCSC Ensembl
Innerchr16:69998220..70046272hg18UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3848053
hg1948053
hg1848053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064435
Supporting Variants
Samples
Known GenesZNF23
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3719027
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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