A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592603



Internal ID20965674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119814108..119815112hg38UCSC Ensembl
chr10:121573620..121574624hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv901n223
Supporting Variantsnssv18231434
Samples
Known GenesINPP5F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592603
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