A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561808



Internal ID20934879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16915763..16920149hg38UCSC Ensembl
chr4:16917386..16921772hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg384387
hg194387
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561808
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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