A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561640



Internal ID20934711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:129885871..129959524hg38UCSC Ensembl
chr4:130807026..130880679hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3873654
hg1973654
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561640
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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