A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568695



Internal ID20941766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:144671919..144672914hg38UCSC Ensembl
chr4:145593071..145594066hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38996
hg19996
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264764
Samples
Known GenesHHIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568695
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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