A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373644



Internal ID22599313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46141546..46142480hg38UCSC Ensembl
chr1:46607218..46608152hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38935
hg19935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875567
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373644
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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