A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458699



Internal ID22516582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22425444..22433100hg38UCSC Ensembl
chr1:22751937..22759593hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg387657
hg197657
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458699
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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