A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560627



Internal ID20933698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76775651..76775862hg38UCSC Ensembl
chr4:77696804..77697015hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265295
Samples
Known GenesSHROOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560627
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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