A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035922



Internal ID18778453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:33373420..34650099hg38UCSC Ensembl
Innerchr12:33526355..34803034hg19UCSC Ensembl
Innerchr12:33417622..34694301hg18UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg381276680
hg191276680
hg181276680
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1432n100
Supporting Variantsnssv3712427, nssv3518371, nssv3508224, nssv3712426, nssv3512167, nssv3513716
Samples
Known GenesALG10, SYT10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035922
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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