A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463193



Internal ID22521078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19036222..19044980hg38UCSC Ensembl
chr1:19362716..19371474hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg388759
hg198759
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828470
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463193
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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