A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024353



Internal ID20591393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36656101..36658400hg38UCSC Ensembl
chr15:36948302..36950601hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512837
Supporting Variants
Samples
Known GenesC15orf41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024353
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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