A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025522



Internal ID20592563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:54409380..54409751hg38UCSC Ensembl
chr15:54701578..54701949hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500157
Supporting Variants
Samples
Known GenesUNC13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025522
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00086


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