A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595077



Internal ID21787120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77526358..77528210hg38UCSC Ensembl
chr9:80141274..80143126hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg381853
hg191853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005416
Supporting Variants
Samples
Known GenesGNA14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595077
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer