A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456792



Internal ID22514672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200524257..200527469hg38UCSC Ensembl
chr1:200493385..200496597hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg383213
hg193213
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828993
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456792
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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