A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557758



Internal ID20930829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20605830..20606476hg38UCSC Ensembl
chr4:20607453..20608099hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265542
Samples
Known GenesSLIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557758
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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