A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577878



Internal ID20950949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27173589..27174031hg38UCSC Ensembl
chr10:27462518..27462960hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv666n223
Supporting Variantsnssv18233628
Samples
Known GenesMASTL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577878
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