A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877279



Internal ID22652242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35354313..35357496hg38UCSC Ensembl
chr17:33681332..33684515hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383184
hg193184
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478152, nssv17478151
Samples
Known GenesSLFN11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877279
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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