A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105184



Internal ID22014417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59600626..59987963hg38UCSC Ensembl
chr17:57677987..58065324hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38387338
hg19387338
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629501
Samples
Known GenesCLTC, DHX40, MIR21, PTRH2, RNFT1, RPS6KB1, TBC1D3P1-DHX40P1, TUBD1, VMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105184
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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