A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480051



Internal ID22537954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:48526418..48530088hg38UCSC Ensembl
chr1:48992090..48995760hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg383671
hg193671
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830224
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480051
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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