A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058736



Internal ID19147955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63260475..63352857hg38UCSC Ensembl
Innerchr16:63294379..63386761hg19UCSC Ensembl
Innerchr16:61851880..61944262hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3892383
hg1992383
hg1892383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2991n100
Supporting Variantsnssv3559381, nssv3559380
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)nsv1058736
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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