A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677595



Internal ID9943700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62443720..62444011hg38UCSC Ensembl
chr2:62670855..62671146hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6060683, essv5847003
SamplesNA18944, NA18945
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677595
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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