A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577117



Internal ID20950188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1889907..1891505hg38UCSC Ensembl
chr17:1793201..1794799hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381599
hg191599
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242112
Samples
Known GenesRPA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577117
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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