A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576655



Internal ID20949726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102525111..102526303hg38UCSC Ensembl
chr10:104284868..104286060hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381193
hg191193
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv875n223
Supporting Variantsnssv18232083
Samples
Known GenesSUFU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576655
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