A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047103



Internal ID19136322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:8259454..8410027hg38UCSC Ensembl
Innerchr12:8412050..8562623hg19UCSC Ensembl
Innerchr12:8303317..8453890hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38150574
hg19150574
hg18150574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1361n100
Supporting Variantsnssv3708242
Samples
Known GenesLINC00937
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047103
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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