A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712866



Internal ID136532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36635264..36641919hg38UCSC Ensembl
chr17:34991722..34998375hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386656
hg196654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712866
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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