A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13973299



Internal ID3975115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129617844..129618789hg38UCSC Ensembl
Innerchr10:129617844..129618789hg38UCSC Ensembl
Outerchr10:129617592..129619074hg38UCSC Ensembl
chr10:131416108..131417053hg19UCSC Ensembl
Innerchr10:131416108..131417053hg19UCSC Ensembl
Outerchr10:131415856..131417338hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624922
Supporting Variants
SamplesHG00404
Known GenesMGMT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13973299
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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