A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877194



Internal ID22652157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:73442660..73467890hg38UCSC Ensembl
chr1:73908343..73933573hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3825231
hg1925231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877194
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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