A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900353



Internal ID1026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24461828..24463062hg38UCSC Ensembl
chr1:24788318..24789552hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381235
hg191235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426675
Supporting Variants
Samples
Known GenesNIPAL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900353
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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