A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747274



Internal ID20523291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7432547..7432625hg38UCSC Ensembl
chr11:7453778..7453856hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291994
Samples
Known GenesSYT9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747274
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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