A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580984



Internal ID20954055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45954984..45956046hg38UCSC Ensembl
chr17:44032350..44033412hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381063
hg191063
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242373
Samples
Known GenesMAPT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580984
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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