A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028676



Internal ID86819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125242219..125243038hg38UCSC Ensembl
chr9:128004498..128005317hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38820
hg19820
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562708
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028676
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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