A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17011128



Internal ID75065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28873839..28873931hg38UCSC Ensembl
chr8:28731356..28731448hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473979
Supporting Variants
Samples
Known GenesINTS9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17011128
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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