A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13904831



Internal ID3906647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95647004..95665355hg38UCSC Ensembl
Innerchr10:95647004..95665355hg38UCSC Ensembl
Outerchr10:95646504..95665855hg38UCSC Ensembl
chr10:97406761..97425112hg19UCSC Ensembl
Innerchr10:97406761..97425112hg19UCSC Ensembl
Outerchr10:97406261..97425612hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3818352
hg1918352
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624282
Supporting Variants
SamplesHG02817
Known GenesALDH18A1, TCTN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13904831
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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