A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023991



Internal ID20591031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43734662..43735950hg38UCSC Ensembl
chr15:44026860..44028148hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg381289
hg191289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506961
Supporting Variants
Samples
Known GenesCATSPER2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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