A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712998



Internal ID136664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38926902..38928803hg38UCSC Ensembl
chr17:37083155..37085056hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533709
Supporting Variants
Samples
Known GenesLINC00672
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712998
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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