A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623077



Internal ID6663245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44960870..44966255hg38UCSC Ensembl
Innerchr10:44960891..44966235hg38UCSC Ensembl
Outerchr10:44960850..44966276hg38UCSC Ensembl
chr10:45456318..45461703hg19UCSC Ensembl
Innerchr10:45456339..45461683hg19UCSC Ensembl
Outerchr10:45456298..45461724hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg385386
hg195386
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13765137, essv13765141, essv13765140, essv13765139, essv13765138
SamplesNA19794, HG00142, HG00306, HG00272, HG00182
Known GenesRASSF4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623077
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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