A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438846



Internal ID217395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230535849..230535933hg38UCSC Ensembl
chr2:231400564..231400648hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16925756
Samples
Known GenesSP100
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438846
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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