A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042364



Internal ID18784895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:8265371..8453233hg38UCSC Ensembl
Innerchr12:8417967..8605829hg19UCSC Ensembl
Innerchr12:8309234..8497096hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38187863
hg19187863
hg18187863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1360n100
Supporting Variantsnssv3708251
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)nsv1042364
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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