A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281381



Internal ID20490599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132723447..132723537hg38UCSC Ensembl
chr10:134536951..134537041hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745191
Supporting Variants
Samples
Known GenesINPP5A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281381
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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