A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637466



Internal ID7024258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100134370..100214593hg38UCSC Ensembl
chr15:100674575..100754798hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3880224
hg1980224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv469e214
Supporting Variantsessv15346840
SamplesHG02384
Known GenesADAMTS17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637466
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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