A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714662



Internal ID138328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75800971..75801575hg38UCSC Ensembl
chr17:73797052..73797656hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515128
Supporting Variants
Samples
Known GenesUNK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714662
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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