A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877937



Internal ID22652903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85982042..85987326hg38UCSC Ensembl
chr2:86209165..86214449hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg385285
hg195285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877937
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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