A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869760



Internal ID22644695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79994486..79994660hg38UCSC Ensembl
chr1:80460171..80460345hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373424
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869760
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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