A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443871



Internal ID222256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65148265..65155843hg38UCSC Ensembl
chr2:65375399..65382977hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg387579
hg197579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16914592
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443871
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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