A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637456



Internal ID7024248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99977248..99978166hg38UCSC Ensembl
Innerchr15:99977298..99978116hg38UCSC Ensembl
Outerchr15:99977198..99978216hg38UCSC Ensembl
chr15:100517453..100518371hg19UCSC Ensembl
Innerchr15:100517503..100518321hg19UCSC Ensembl
Outerchr15:100517403..100518421hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15346497, essv15346498
SamplesNA20895, HG03258
Known GenesADAMTS17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637456
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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