A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624424



Internal ID6664590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103971385..103974772hg38UCSC Ensembl
Innerchr10:103971450..103974707hg38UCSC Ensembl
Outerchr10:103971320..103974837hg38UCSC Ensembl
chr10:105731143..105734530hg19UCSC Ensembl
Innerchr10:105731208..105734465hg19UCSC Ensembl
Outerchr10:105731078..105734595hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg383388
hg193388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13915189, essv13915190
SamplesHG04177, HG03914
Known GenesSLK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624424
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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