A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571753



Internal ID20944824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166389780..166390945hg38UCSC Ensembl
chr4:167310932..167312097hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571753
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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