A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437725



Internal ID216309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67916409..67924426hg38UCSC Ensembl
chr2:68143541..68151558hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg388018
hg198018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16915045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437725
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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