A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912998



Internal ID22688214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132540992..132541107hg38UCSC Ensembl
chr10:134354496..134354611hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350981
Samples
Known GenesINPP5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912998
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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