A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468130



Internal ID22526019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132552232..132554468hg38UCSC Ensembl
chr10:134365736..134367972hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382237
hg192237
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851885
Supporting Variants
Samples
Known GenesINPP5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468130
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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