A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513649



Internal ID20886995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89463164..89464501hg38UCSC Ensembl
chr15:90006395..90007732hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381338
hg191338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513649
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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