A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560676



Internal ID20933747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39531616..39532792hg38UCSC Ensembl
chr4:39533236..39534412hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381177
hg191177
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265160
Samples
Known GenesMIR1273H, UGDH-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560676
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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