A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459080



Internal ID22516962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205472338..205474530hg38UCSC Ensembl
chr1:205441466..205443658hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382193
hg192193
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829167
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459080
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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