A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506624



Internal ID283364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132572963..132574316hg38UCSC Ensembl
chr10:134386467..134387820hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381354
hg191354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042388
Samples
Known GenesINPP5A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506624
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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