A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660836



Internal ID9926941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37709942..37717167hg38UCSC Ensembl
chr1:38175614..38182839hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg387226
hg197226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6401521
SamplesNA19404
Known GenesEPHA10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660836
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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