A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024751



Internal ID20591791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48780249..48780759hg38UCSC Ensembl
chr15:49072446..49072956hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513407
Supporting Variants
Samples
Known GenesCEP152
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0008


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