A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024557



Internal ID20591597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43971501..43973500hg38UCSC Ensembl
chr15:44263699..44265698hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511399
Supporting Variants
Samples
Known GenesFRMD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024557
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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