A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580514



Internal ID20953585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39075117..39075774hg38UCSC Ensembl
chr17:37231370..37232027hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242254
Samples
Known GenesLOC100131347, PLXDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580514
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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