A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6449259



Internal ID9426662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74577..76650hg38UCSC Ensembl
chr5:74692..76765hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382074
hg192074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677502
Supporting Variants
SamplesNA18502
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6449259
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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