A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711214



Internal ID134880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7615553..7616660hg38UCSC Ensembl
chr17:7518871..7519978hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381108
hg191108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524911
Supporting Variants
Samples
Known GenesSHBG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711214
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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