A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978565



Internal ID20545605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132665297..132665778hg38UCSC Ensembl
chr10:134478801..134479282hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438435
Supporting Variants
Samples
Known GenesINPP5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00199


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