A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883702



Internal ID22658684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110930069..110935090hg38UCSC Ensembl
chr1:111472691..111477712hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg385022
hg195022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883702
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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