A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567827



Internal ID20940898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70744805..70745804hg38UCSC Ensembl
chr4:71610522..71611521hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5329n223
Supporting Variantsnssv18265963
Samples
Known GenesRUFY3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567827
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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