A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584378



Internal ID21776421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132540991..132541108hg38UCSC Ensembl
chr10:134354495..134354612hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012303
Supporting Variants
Samples
Known GenesINPP5A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584378
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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