A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435871



Internal ID214501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186522196..186541181hg38UCSC Ensembl
chr2:187386923..187405908hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3818986
hg1918986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16922776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5435871
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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