A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711530



Internal ID135196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13099361..13099694hg38UCSC Ensembl
chr17:13002678..13003011hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529773
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711530
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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