A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737596



Internal ID20513558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55618569..55618688hg38UCSC Ensembl
chr4:56484736..56484855hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268663
Samples
Known GenesNMU
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737596
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