A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872779



Internal ID22647720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234740285..234742393hg38UCSC Ensembl
chr1:234876032..234878140hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg382109
hg192109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872779
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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