A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508161



Internal ID20881459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59333855..59351988hg38UCSC Ensembl
chr15:59626054..59644187hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3818134
hg1918134
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180286
Samples
Known GenesMYO1E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508161
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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