A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353476



Internal ID22579145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23618259..23622979hg38UCSC Ensembl
chr1:23944749..23949469hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384721
hg194721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872134
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353476
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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