A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459733



Internal ID22517619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207842380..207847857hg38UCSC Ensembl
chr1:208015725..208021202hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg385478
hg195478
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829175
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459733
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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