A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462959



Internal ID22520844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182114666..182118565hg38UCSC Ensembl
chr1:182083801..182087700hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828766
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462959
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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