A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670070



Internal ID9936175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:12099347..12099679hg38UCSC Ensembl
Outerchr6:12099310..12099729hg38UCSC Ensembl
Innerchr6:12099580..12099912hg19UCSC Ensembl
Outerchr6:12099543..12099962hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38420
hg19420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5950116
SamplesNA18868
Known GenesHIVEP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670070
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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