A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990223



Internal ID20557265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29453458..29453976hg38UCSC Ensembl
chr11:29475005..29475523hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442240
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990223
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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