A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193004



Internal ID20760045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77272293..77273050hg38UCSC Ensembl
chr11:76983338..76984095hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466293
Supporting Variants
Samples
Known GenesGDPD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193004
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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