A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565862



Internal ID20938933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15770084..15770391hg38UCSC Ensembl
chr4:15771707..15772014hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565862
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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