A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677868



Internal ID9597287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33160969..33161762hg38UCSC Ensembl
chr19:33651875..33652668hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5902174, essv5900928, essv5711350, essv5871880, essv6034263, essv6046668, essv6238562, essv5929007, essv5814556, essv5559544, essv5720656, essv6454934, essv5958650, essv6363119, essv5436065, essv5666489, essv6052580, essv6023906
SamplesNA18964, NA18570, NA19003, HG00614, HG00592, HG00593, NA18566, NA18536, NA19055, NA19080, HG00653, HG00672, HG00427, HG00595, NA18611, NA11829, HG00473, HG00476
Known GenesWDR88
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677868
Frequency
Sample Size1151
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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