A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425067



Internal ID22482937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:27189243..27189243hg38UCSC Ensembl
chr4:27190865..27190865hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5953345
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425067
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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