A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572520



Internal ID20945591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23604700..23606145hg38UCSC Ensembl
chr7:23644319..23645764hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381446
hg191446
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272722
Samples
Known GenesCCDC126
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572520
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