A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882901



Internal ID22657878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45611745..45612151hg38UCSC Ensembl
chr1:46077417..46077823hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370325
Samples
Known GenesNASP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882901
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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