A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583196



Internal ID20956267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14204036..14435006hg38UCSC Ensembl
chr17:14107353..14338323hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38230971
hg19230971
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241358
Samples
Known GenesCDRT15, COX10, HS3ST3B1, MGC12916
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583196
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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