A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985375



Internal ID20552415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9186120..9189237hg38UCSC Ensembl
chr10:9228083..9231200hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383118
hg193118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453770
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00128


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer