A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13704099



Internal ID6069955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15430683..15435623hg38UCSC Ensembl
Innerchr10:15430720..15435587hg38UCSC Ensembl
Outerchr10:15430647..15435660hg38UCSC Ensembl
chr10:15472682..15477622hg19UCSC Ensembl
Innerchr10:15472719..15477586hg19UCSC Ensembl
Outerchr10:15472646..15477659hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384941
hg194941
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622444
Supporting Variants
SamplesNA19457
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13704099
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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