A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049872



Internal ID19139091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31849350..31908234hg38UCSC Ensembl
Innerchr12:32002284..32061168hg19UCSC Ensembl
Innerchr12:31893551..31952435hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3858885
hg1958885
hg1858885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1426n100
Supporting Variantsnssv3512331
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)nsv1049872
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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