A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042920



Internal ID19132139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:28731593..28791193hg38UCSC Ensembl
Innerchr12:28884526..28944126hg19UCSC Ensembl
Innerchr12:28775793..28835393hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3859601
hg1959601
hg1859601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514566
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)nsv1042920
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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