A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362982



Internal ID22588651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:116571269..116571321hg38UCSC Ensembl
chr1:117113891..117113943hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884987
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362982
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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