A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450261



Internal ID22508131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173161877..173164206hg38UCSC Ensembl
chr1:173131016..173133345hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg382330
hg192330
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828735
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450261
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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