A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624407



Internal ID6664574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103172847..103174048hg38UCSC Ensembl
Innerchr10:103172897..103173998hg38UCSC Ensembl
Outerchr10:103172797..103174098hg38UCSC Ensembl
chr10:104932604..104933805hg19UCSC Ensembl
Innerchr10:104932654..104933755hg19UCSC Ensembl
Outerchr10:104932554..104933855hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13913937
SamplesHG00731
Known GenesNT5C2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624407
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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