A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624082



Internal ID7010938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86111693..86115778hg38UCSC Ensembl
Innerchr10:86111726..86115746hg38UCSC Ensembl
Outerchr10:86111661..86115811hg38UCSC Ensembl
chr10:87871450..87875535hg19UCSC Ensembl
Innerchr10:87871483..87875503hg19UCSC Ensembl
Outerchr10:87871418..87875568hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg384086
hg194086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13883020
SamplesHG03914
Known GenesGRID1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624082
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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