A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv469e214



Internal ID22756363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100134370..100237690hg38UCSC Ensembl
chr15:100674575..100777895hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38103321
hg19103321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3637466, esv3637468
SamplesHG02384
Known GenesADAMTS17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv469e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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