A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038938



Internal ID19128157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:37463949..37687469hg38UCSC Ensembl
Innerchr12:37857751..38081271hg19UCSC Ensembl
Innerchr12:36144018..36367538hg18UCSC Ensembl
Cytoband12q11
Allele length
AssemblyAllele length
hg38223521
hg19223521
hg18223521
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1466n100
Supporting Variantsnssv3522865
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)nsv1038938
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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