A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438551



Internal ID22496421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89841277..89841424hg38UCSC Ensembl
chr6:90550996..90551143hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893915
Supporting Variants
Samples
Known GenesCASP8AP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438551
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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