A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375452



Internal ID22601121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:68642948..68644065hg38UCSC Ensembl
chr1:69108631..69109748hg19UCSC Ensembl
Cytoband1p31.2
Allele length
AssemblyAllele length
hg381118
hg191118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882792
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375452
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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