A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748619



Internal ID21390875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42869830..42871804hg38UCSC Ensembl
chr6:42837568..42839542hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381975
hg191975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434975
Supporting Variants
SamplesNB12
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748619
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