A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576783



Internal ID20949854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48836906..48837457hg38UCSC Ensembl
chr17:46914268..46914819hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244480
Samples
Known GenesCALCOCO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576783
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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