A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571519



Internal ID20944590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153753557..153754185hg38UCSC Ensembl
chr4:154674709..154675337hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263901
Samples
Known GenesRNF175
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571519
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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