A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463404



Internal ID21120957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77230988..77239706hg38UCSC Ensembl
chr11:76942033..76950751hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg388719
hg198719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994132
Samples
Known GenesGDPD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463404
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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