A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010199



Internal ID74433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21725283..21750085hg38UCSC Ensembl
chr8:21582795..21607597hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3824803
hg1924803
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559815
Supporting Variants
Samples
Known GenesGFRA2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010199
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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