A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713017



Internal ID136683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39160269..39172978hg38UCSC Ensembl
chr17:37316522..37329231hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3812710
hg1912710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532076
Supporting Variants
Samples
Known GenesARL5C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713017
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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