A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468348



Internal ID22526237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161027660..161029354hg38UCSC Ensembl
chr1:160997450..160999144hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg381695
hg191695
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828380
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468348
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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