A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355269



Internal ID22580938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16166185..16166240hg38UCSC Ensembl
chr1:16492680..16492735hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867891
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355269
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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