A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375944



Internal ID22601613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7571836..7571888hg38UCSC Ensembl
chr17:7475154..7475206hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934993
Supporting Variants
Samples
Known GenesSENP3, SENP3-EIF4A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375944
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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