A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481602



Internal ID22539506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96266202..96269316hg38UCSC Ensembl
chr1:96731758..96734872hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg383115
hg193115
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831048
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481602
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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