A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267709



Internal ID20476927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19025181..19149357hg38UCSC Ensembl
chr17:18928494..19052670hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38124177
hg19124177
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755191
Supporting Variants
Samples
Known GenesGRAP, GRAPL
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267709
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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