A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637452



Internal ID6677556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99956434..99973828hg38UCSC Ensembl
chr15:100496639..100514033hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3817395
hg1917395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15346486, essv15346483, essv15346485, essv15346487, essv15346482, essv15346484, essv15346481
SamplesNA19028, NA19141, HG02678, NA19834, HG00620, HG04171, NA18488
Known GenesADAMTS17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637452
Frequency
Sample Size2504
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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