A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711751



Internal ID135417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15979673..15979912hg38UCSC Ensembl
chr17:15882987..15883226hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530112
Supporting Variants
Samples
Known GenesZSWIM7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711751
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.035759


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