A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451835



Internal ID22509707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244874433..244875841hg38UCSC Ensembl
chr1:245037735..245039143hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg381409
hg191409
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829589
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451835
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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