A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285725



Internal ID20494943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98393017..98393180hg38UCSC Ensembl
chr7:98022329..98022492hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747748
Supporting Variants
Samples
Known GenesBAIAP2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285725
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