A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676719



Internal ID9942824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93543916..93546584hg38UCSC Ensembl
chr7:93173228..93175896hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382669
hg192669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5712961
SamplesNA19130
Known GenesCALCR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676719
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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