A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457672



Internal ID22515553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183614519..183615570hg38UCSC Ensembl
chr1:183583654..183584705hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg381052
hg191052
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828769
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457672
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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