A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13913866



Internal ID3915682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102875502..102882024hg38UCSC Ensembl
Innerchr10:102876002..102881524hg38UCSC Ensembl
Outerchr10:102874502..102883024hg38UCSC Ensembl
chr10:104635259..104641781hg19UCSC Ensembl
Innerchr10:104635759..104641281hg19UCSC Ensembl
Outerchr10:104634259..104642781hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg386523
hg196523
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624404
Supporting Variants
SamplesNA19351
Known GenesAS3MT, C10orf32-ASMT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13913866
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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