A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622497



Internal ID7009356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17706450..17707963hg38UCSC Ensembl
Innerchr10:17706500..17707914hg38UCSC Ensembl
Outerchr10:17706401..17708013hg38UCSC Ensembl
chr10:17748449..17749962hg19UCSC Ensembl
Innerchr10:17748499..17749913hg19UCSC Ensembl
Outerchr10:17748400..17750012hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg381514
hg191514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13707433, essv13707434
SamplesHG02682, HG02681
Known GenesSTAM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622497
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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