A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503934



Internal ID20877192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61010597..61011052hg38UCSC Ensembl
chr15:61302796..61303251hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026063
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503934
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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