A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622444



Internal ID7009303
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13704098, essv13704099
SamplesNA19457, HG02635
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622444
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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