A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623159



Internal ID6663327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48883503..48885965hg38UCSC Ensembl
Innerchr10:48883516..48885953hg38UCSC Ensembl
Outerchr10:48883491..48885978hg38UCSC Ensembl
chr10:50091548..50094010hg19UCSC Ensembl
Innerchr10:50091561..50093998hg19UCSC Ensembl
Outerchr10:50091536..50094023hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg382463
hg192463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13796100
SamplesHG03814
Known GenesWDFY4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623159
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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