A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17042385



Internal ID95973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132552103..132552729hg38UCSC Ensembl
chr10:134365607..134366233hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504367
Supporting Variants
Samples
Known GenesINPP5A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17042385
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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