A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274416



Internal ID20483634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55105986..55106249hg38UCSC Ensembl
chr5:54401814..54402077hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731801
Supporting Variants
Samples
Known GenesGZMA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274416
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