A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747682



Internal ID20523702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73956989..73957040hg38UCSC Ensembl
chr13:74531126..74531177hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284087
Samples
Known GenesKLF12
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747682
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