A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052157



Internal ID19141376
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 StatusM
Merged Variantsdgv2789n100
Supporting Variantsnssv3542794, nssv3542788, nssv3542789, nssv3542793, nssv3542792, nssv3542791, nssv3542790
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)nsv1052157
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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