A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154782



Internal ID20721822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18021035..18027902hg38UCSC Ensembl
chr7:18060658..18067525hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg386868
hg196868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615054
Supporting Variants
Samples
Known GenesPRPS1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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