A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481098



Internal ID22539002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62013389..62015038hg38UCSC Ensembl
chr1:62479061..62480710hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830108
Supporting Variants
Samples
Known GenesINADL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481098
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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