A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357613



Internal ID22583282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154917756..154918672hg38UCSC Ensembl
chr1:154890232..154891148hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877978
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357613
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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