A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713061



Internal ID136727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39850080..39850182hg38UCSC Ensembl
chr17:38006333..38006435hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145523
Supporting Variants
Samples
Known GenesIKZF3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713061
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.193838


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