A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674938



Internal ID9941043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:7731501..7739225hg38UCSC Ensembl
chr2:7871632..7879356hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg387725
hg197725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5854368
SamplesNA19371
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674938
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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