A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466791



Internal ID22524682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21785134..21789149hg38UCSC Ensembl
chr1:22111627..22115642hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg384016
hg194016
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828895
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466791
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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