A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021523



Internal ID81995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34985634..34985695hg38UCSC Ensembl
chr9:34985631..34985692hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476021
Supporting Variants
Samples
Known GenesLOC101926900
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021523
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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