A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502175



Internal ID20875418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60660601..60661400hg38UCSC Ensembl
chr15:60952800..60953599hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026046
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502175
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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