A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000495



Internal ID67908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100117686..100117708hg38UCSC Ensembl
chr7:99715309..99715331hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3823
hg1923
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554296
Supporting Variants
Samples
Known GenesTAF6
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000495
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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