A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579318



Internal ID20952389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72765738..72765823hg38UCSC Ensembl
chr10:74525496..74525581hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234968
Samples
Known GenesMCU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579318
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