A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025264



Internal ID84569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74371472..74378348hg38UCSC Ensembl
chr9:76986388..76993264hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg386877
hg196877
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147016
Supporting Variants
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025264
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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