A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262782



Internal ID20472000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56635262..56635262hg38UCSC Ensembl
chr19:57146630..57146630hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262782
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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