A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494734



Internal ID271867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110912091..110912961hg38UCSC Ensembl
chr10:112671849..112672719hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041093
Samples
Known GenesBBIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494734
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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