A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574547



Internal ID20947618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70715888..70716253hg38UCSC Ensembl
chr4:71581605..71581970hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265959
Samples
Known GenesRUFY3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574547
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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