A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871818



Internal ID22646756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31740940..31741028hg38UCSC Ensembl
chr2:31966009..31966097hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393181
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871818
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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