A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671717



Internal ID9937822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140993580..140995343hg38UCSC Ensembl
chr7:140693380..140695143hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381764
hg191764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6348958
SamplesHG00732
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671717
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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