A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515219



Internal ID20888578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74392976..74394565hg38UCSC Ensembl
chr15:74685316..74686905hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381590
hg191590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026664
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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