A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481056



Internal ID22538960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54898239..54903485hg38UCSC Ensembl
chr1:55363912..55369158hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg385247
hg195247
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830399
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481056
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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