A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361631



Internal ID22587300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117050785..117052321hg38UCSC Ensembl
chr1:117593407..117594943hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg381537
hg191537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361631
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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