A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871085



Internal ID22646023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60086394..60098783hg38UCSC Ensembl
chr1:60552066..60564455hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3812390
hg1912390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371929
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871085
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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