A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409147



Internal ID22467017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86821117..86821412hg38UCSC Ensembl
chr1:87286800..87287095hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882403
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409147
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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