A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979155



Internal ID20546195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21349203..21364671hg38UCSC Ensembl
chr10:21638132..21653600hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3815469
hg1915469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443605
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979155
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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