A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577004



Internal ID20950075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4446415..4543429hg38UCSC Ensembl
chr10:4488607..4585621hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3897015
hg1997015
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577004
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