A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900230



Internal ID945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25567440..25567488hg38UCSC Ensembl
chr1:25893931..25893979hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539185
Supporting Variants
Samples
Known GenesLDLRAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900230
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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