A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281954



Internal ID20491172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91585631..91592140hg38UCSC Ensembl
chr7:91214946..91221455hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg386510
hg196510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735624
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281954
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