A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147016



Internal ID346222
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 StatusM
Merged Variants
Supporting Variantsnssv17025264
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147016
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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