A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043626



Internal ID18786157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:18564935..18780530hg38UCSC Ensembl
Innerchr16:18576257..18791852hg19UCSC Ensembl
Innerchr16:18483758..18699353hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38215596
hg19215596
hg18215596
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2786n100
Supporting Variantsnssv3542764, nssv3542765, nssv3542766
Samples
Known GenesABCC6P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043626
Frequency
Sample Size29084
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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