A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981354



Internal ID20548394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29547671..29548162hg38UCSC Ensembl
chr10:29836600..29837091hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452290
Supporting Variants
Samples
Known GenesSVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981354
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0005


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