A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506582



Internal ID20879864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90899259..90900342hg38UCSC Ensembl
chr15:91442489..91443572hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381084
hg191084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027400
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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