A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623815



Internal ID7010671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73568425..73570524hg38UCSC Ensembl
Innerchr10:73568431..73570518hg38UCSC Ensembl
Outerchr10:73568419..73570530hg38UCSC Ensembl
chr10:75328183..75330282hg19UCSC Ensembl
Innerchr10:75328189..75330276hg19UCSC Ensembl
Outerchr10:75328177..75330288hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13861916
SamplesHG02614
Known GenesUSP54
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623815
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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