A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874475



Internal ID22649427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85264940..85265117hg38UCSC Ensembl
chr1:85730623..85730800hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384124
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874475
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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