A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623084



Internal ID6663252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45150201..45157651hg38UCSC Ensembl
Innerchr10:45150266..45157587hg38UCSC Ensembl
Outerchr10:45150137..45157716hg38UCSC Ensembl
chr10:45645649..45653099hg19UCSC Ensembl
Innerchr10:45645714..45653035hg19UCSC Ensembl
Outerchr10:45645585..45653164hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg387451
hg197451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13770154, essv13770155
SamplesHG03380, HG02397
Known GenesANKRD30BP3, RSU1P2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623084
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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