A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560586



Internal ID20933657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99933336..99934635hg38UCSC Ensembl
chr4:100854493..100855792hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266135
Samples
Known GenesDNAJB14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560586
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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