A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622515



Internal ID7009374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18717945..18755799hg38UCSC Ensembl
Innerchr10:18717945..18755799hg38UCSC Ensembl
Outerchr10:18717445..18756299hg38UCSC Ensembl
chr10:19006874..19044728hg19UCSC Ensembl
Innerchr10:19006874..19044728hg19UCSC Ensembl
Outerchr10:19006374..19045228hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3837855
hg1937855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13710231
SamplesNA20802
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622515
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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