A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459881



Internal ID22517767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154670794..154678563hg38UCSC Ensembl
chr1:154643270..154651039hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg387770
hg197770
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828151
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459881
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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