A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587821



Internal ID20960892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14861934..14862135hg38UCSC Ensembl
chr10:14903933..14904134hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224229
Samples
Known GenesHSPA14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587821
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