A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269334



Internal ID20478552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119794776..119794884hg38UCSC Ensembl
chr10:121554288..121554396hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733461
Supporting Variants
Samples
Known GenesINPP5F
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269334
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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