A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171550



Internal ID20738590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100451609..100471804hg38UCSC Ensembl
chr9:103213891..103234086hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3820196
hg1920196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448725
Supporting Variants
Samples
Known GenesMSANTD3, MSANTD3-TMEFF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171550
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