A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592199



Internal ID20965270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63123290..63123817hg38UCSC Ensembl
chr17:61200651..61201178hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242604
Samples
Known GenesMIR548W, TANC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592199
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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