A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17393834



Internal ID22451704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173154087..173154087hg38UCSC Ensembl
chr2:174018815..174018815hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5965051
Supporting Variants
Samples
Known GenesZAK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17393834
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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