A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997958



Internal ID21907301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7230231..7230294hg38UCSC Ensembl
chr4:7231958..7232021hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551186
Samples
Known GenesSORCS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997958
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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