A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585074



Internal ID20958145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44799251..44799878hg38UCSC Ensembl
chr17:42876619..42877246hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242342
Samples
Known GenesGJC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585074
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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