A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039361



Internal ID93963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119814118..119814118hg38UCSC Ensembl
chr10:121573630..121573630hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544718
Supporting Variants
Samples
Known GenesINPP5F
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039361
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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