A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629949



Internal ID21821996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60019185..60110888hg38UCSC Ensembl
chr17:58096546..58188249hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg3891704
hg1991704
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110284
Supporting Variants
Samples
Known GenesHEATR6, LOC645638, LOC653653, MIR4737
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629949
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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