A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6235965



Internal ID9115935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:128188715..128189380hg38UCSC Ensembl
Outerchr12:128188676..128189437hg38UCSC Ensembl
Innerchr12:128673260..128673925hg19UCSC Ensembl
Outerchr12:128673221..128673982hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675404
Supporting Variants
SamplesHG01124
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6235965
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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