A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478037



Internal ID255601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101822583..101822655hg38UCSC Ensembl
chr10:103582340..103582412hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037648
Samples
Known GenesKCNIP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478037
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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