A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036596



Internal ID19125815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:37640544..38031180hg38UCSC Ensembl
Innerchr12:38034346..38424982hg19UCSC Ensembl
Innerchr12:36320613..36711249hg18UCSC Ensembl
Cytoband12q11
Allele length
AssemblyAllele length
hg38390637
hg19390637
hg18390637
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1470n100
Supporting Variantsnssv3522955
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)nsv1036596
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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