A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878509



Internal ID22653475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157967710..157967812hg38UCSC Ensembl
chr1:157937500..157937602hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878509
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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