A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665526



Internal ID9931631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179915030..179917298hg38UCSC Ensembl
chr5:179342030..179344298hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg382269
hg192269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5809912, essv6085005, essv6508136, essv5615072
SamplesNA19355, HG01198, NA19398, HG00274
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665526
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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