A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273071



Internal ID20482289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74202195..74202581hg38UCSC Ensembl
chr7:73616525..73616911hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741849
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273071
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