A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670726



Internal ID9936831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15678997..15679208hg38UCSC Ensembl
chr2:15819121..15819332hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5681755, essv6379257, essv6033637
SamplesHG00318, NA12891, HG00275
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670726
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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