A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027392



Internal ID20594432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90834625..90837966hg38UCSC Ensembl
chr15:91377855..91381196hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383342
hg193342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514107
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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