A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187152



Internal ID20754192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74903376..74903740hg38UCSC Ensembl
chr9:77518292..77518656hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437315
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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