A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624387



Internal ID7011243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101685852..101686462hg38UCSC Ensembl
Innerchr10:101685967..101686412hg38UCSC Ensembl
Outerchr10:101685701..101686613hg38UCSC Ensembl
chr10:103445609..103446219hg19UCSC Ensembl
Innerchr10:103445724..103446169hg19UCSC Ensembl
Outerchr10:103445458..103446370hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13913607, essv13913609, essv13913603, essv13913604, essv13913605, essv13913606, essv13913608
SamplesNA11920, HG03888, HG03771, NA20767, NA20881, HG00254, NA20786
Known GenesFBXW4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624387
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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