A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624233



Internal ID7011089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92986619..92992149hg38UCSC Ensembl
Innerchr10:92986619..92992149hg38UCSC Ensembl
Outerchr10:92986434..92992332hg38UCSC Ensembl
chr10:94746376..94751906hg19UCSC Ensembl
Innerchr10:94746376..94751906hg19UCSC Ensembl
Outerchr10:94746191..94752089hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg385531
hg195531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13899274
SamplesNA18638
Known GenesEXOC6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624233
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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