A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381416



Internal ID22439286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42466114..42471557hg38UCSC Ensembl
chr1:42931785..42937228hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg385444
hg195444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884760
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381416
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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