A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437262



Internal ID215856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161620762..161893078hg38UCSC Ensembl
chr2:162477272..162749588hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38272317
hg19272317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16920261
Samples
Known GenesSLC4A10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437262
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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