A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666095



Internal ID9932200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:61407892..61413444hg38UCSC Ensembl
Outerchr2:61407855..61413494hg38UCSC Ensembl
Innerchr2:61635027..61640579hg19UCSC Ensembl
Outerchr2:61634990..61640629hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg385640
hg195640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5642070
SamplesNA20809
Known GenesUSP34
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666095
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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