A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024556



Internal ID20591596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43989879..44128614hg38UCSC Ensembl
chr15:44282077..44420812hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38138736
hg19138736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496732
Supporting Variants
Samples
Known GenesFRMD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024556
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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