A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557531



Internal ID20930602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106558765..107137678hg38UCSC Ensembl
chr4:107479922..108058835hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38578914
hg19578914
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263453
Samples
Known GenesDKK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557531
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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