A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17378450



Internal ID22436320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32976485..32979369hg38UCSC Ensembl
chr1:33442086..33444970hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382885
hg192885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876458
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17378450
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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