A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637442



Internal ID7024234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99877102..100060087hg38UCSC Ensembl
chr15:100417307..100600292hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38182986
hg19182986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15346428, essv15346429
SamplesNA20294, HG01464
Known GenesADAMTS17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637442
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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