A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575677



Internal ID20948748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11941278..12109821hg38UCSC Ensembl
chr17:11844595..12013138hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38168544
hg19168544
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240991
Samples
Known GenesDNAH9, MAP2K4, MIR744, ZNF18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575677
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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