A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038702



Internal ID19127921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:37463949..37640544hg38UCSC Ensembl
Innerchr12:37857751..38034346hg19UCSC Ensembl
Innerchr12:36144018..36320613hg18UCSC Ensembl
Cytoband12q11
Allele length
AssemblyAllele length
hg38176596
hg19176596
hg18176596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1465n100
Supporting Variantsnssv3522862
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)nsv1038702
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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