A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662183



Internal ID9581602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1079149..1079449hg38UCSC Ensembl
chr10:1125089..1125389hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6590443, essv5938630, essv6249682, essv6233332
SamplesNA20281, NA19398, NA18909, NA18853
Known GenesWDR37
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662183
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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