A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563514



Internal ID20936585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169858740..169860003hg38UCSC Ensembl
chr5:169285744..169287007hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg381264
hg191264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267624
Samples
Known GenesDOCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563514
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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