A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560675



Internal ID20933746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103053983..103054504hg38UCSC Ensembl
chr4:103975140..103975661hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263405
Samples
Known GenesSLC9B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560675
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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