A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883254



Internal ID22658232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154393910..154394245hg38UCSC Ensembl
chr1:154366386..154366721hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352124
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883254
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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