A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271059



Internal ID20480277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84089880..84099370hg38UCSC Ensembl
chr7:83719196..83728686hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg389491
hg199491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743202
Supporting Variants
Samples
Known GenesSEMA3A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271059
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