A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024602



Internal ID20591642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45169972..45172407hg38UCSC Ensembl
chr15:45462170..45464605hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg382436
hg192436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497774
Supporting Variants
Samples
Known GenesSHF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024602
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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