A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674210



Internal ID9940315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32212743..32213580hg38UCSC Ensembl
chr19:32703649..32704486hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5905534, essv5679707, essv5418581, essv5659409, essv6204992, essv5746214, essv5630014, essv5983422, essv5738372, essv6372524, essv5474308, essv5432629
SamplesNA19700, NA19350, NA19190, NA19920, NA19379, NA18519, NA19313, NA19461, NA19435, NA19439, NA19312, NA19429
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674210
Frequency
Sample Size1151
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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