A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099283



Internal ID21512771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3052058..3252221hg38UCSC Ensembl
chr17:2955352..3155515hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38200164
hg19200164
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668436
Supporting Variants
Samples
Known GenesOR1A1, OR1A2, OR1D2, OR1D4, OR1D5, OR1G1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099283
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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