A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624817



Internal ID7011667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124787173..124792946hg38UCSC Ensembl
Innerchr10:124787223..124792896hg38UCSC Ensembl
Outerchr10:124787123..124792996hg38UCSC Ensembl
chr10:126475742..126481515hg19UCSC Ensembl
Innerchr10:126475792..126481465hg19UCSC Ensembl
Outerchr10:126475692..126481565hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg385774
hg195774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13963335
SamplesHG03303
Known GenesMETTL10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624817
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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