A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461142



Internal ID22519025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17459337..17464857hg38UCSC Ensembl
chr1:17785833..17791353hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg385521
hg195521
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828741
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461142
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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