A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558029



Internal ID20931100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173389539..173390041hg38UCSC Ensembl
chr4:174310690..174311192hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264473
Samples
Known GenesSCRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558029
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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