A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622817



Internal ID7009675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31845605..31854249hg38UCSC Ensembl
Innerchr10:31845658..31854197hg38UCSC Ensembl
Outerchr10:31845553..31854302hg38UCSC Ensembl
chr10:32134533..32143177hg19UCSC Ensembl
Innerchr10:32134586..32143125hg19UCSC Ensembl
Outerchr10:32134481..32143230hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg388645
hg198645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13749656
SamplesHG00589
Known GenesARHGAP12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622817
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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