A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514184



Internal ID20887536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92003669..92008946hg38UCSC Ensembl
chr15:92546899..92552176hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg385278
hg195278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027275
Samples
Known GenesSLCO3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514184
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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