A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670292



Internal ID9936397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90675943..90679565hg38UCSC Ensembl
chr15:91219174..91222796hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383623
hg193623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5562219, essv6278564, essv6132654, essv5625586, essv6353847, essv5399642
SamplesNA19393, NA19457, NA19682, NA19435, NA19360, NA19312
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670292
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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