A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035849



Internal ID18778380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:37535425..38246811hg38UCSC Ensembl
Innerchr12:37929227..38640613hg19UCSC Ensembl
Innerchr12:36215494..36926880hg18UCSC Ensembl
Cytoband12q11
Allele length
AssemblyAllele length
hg38711387
hg19711387
hg18711387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1467n100
Supporting Variantsnssv3522870
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)nsv1035849
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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