A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106037



Internal ID22015270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3070906..3291758hg38UCSC Ensembl
chr17:2974200..3195052hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38220853
hg19220853
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629632
Samples
Known GenesOR1A1, OR1A2, OR1D2, OR1D4, OR1G1, OR3A1, OR3A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106037
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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