A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557574



Internal ID20930645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24913766..25475670hg38UCSC Ensembl
chr4:24915388..25477292hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38561905
hg19561905
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265618
Samples
Known GenesANAPC4, CCDC149, LGI2, PI4K2B, SEPSECS, SEPSECS-AS1, ZCCHC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557574
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer