A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748904



Internal ID21392712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19776609..19777405hg38UCSC Ensembl
chr11:19798155..19798951hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38797
hg19797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431477
Supporting Variants
SamplesSMI041
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748904
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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