A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458506



Internal ID22516389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23653532..23659450hg38UCSC Ensembl
chr1:23980022..23985940hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385919
hg195919
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829411
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458506
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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