A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17393181



Internal ID22451051
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 StatusS
Merged Variantsnsv5871818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17393181
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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