A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027151



Internal ID20594191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95500201..95501500hg38UCSC Ensembl
chr15:96043430..96044729hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499431
Supporting Variants
Samples
Known GenesLINC00924
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01471


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