A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467105



Internal ID22524997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:187072314..187075597hg38UCSC Ensembl
chr1:187041446..187044729hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg383284
hg193284
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828445
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467105
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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