A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676888



Internal ID9596307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:85620401..85622327hg38UCSC Ensembl
chr10:87380158..87382084hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381927
hg191927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5972331, essv5869341, essv6237840, essv5595320
SamplesNA12154, NA20585, HG01102, NA19661
Known GenesGRID1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676888
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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