A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052006



Internal ID20619046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153988289..153989303hg38UCSC Ensembl
chr1:153960765..153961779hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381015
hg191015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316956
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052006
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.07503


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