A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560947



Internal ID20934018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52838442..52839206hg38UCSC Ensembl
chr4:53704609..53705373hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560947
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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