A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025529



Internal ID20592570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:54463657..54750578hg38UCSC Ensembl
chr15:54755855..55042776hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38286922
hg19286922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500825
Supporting Variants
Samples
Known GenesUNC13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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