A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036482



Internal ID18779013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:97620633..97672233hg38UCSC Ensembl
Innerchr12:98014411..98066011hg19UCSC Ensembl
Innerchr12:96538542..96590142hg18UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3851601
hg1951601
hg1851601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1548n100
Supporting Variantsnssv3524842
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)nsv1036482
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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