A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583663



Internal ID20956734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12570816..12571240hg38UCSC Ensembl
chr17:12474133..12474557hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244379
Samples
Known GenesLINC00670
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583663
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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