A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711056



Internal ID134722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5430070..5430369hg38UCSC Ensembl
chr17:5333390..5333689hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521965
Supporting Variants
Samples
Known GenesRPAIN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711056
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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