A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677528



Internal ID2910615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62665900..62671133hg38UCSC Ensembl
chr10:64425660..64430893hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg385234
hg195234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5835093, essv6071050, essv5999640, essv5855860, essv5505752
SamplesNA19114, NA19920, NA19834, HG01108, HG01377
Known GenesZNF365
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677528
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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