A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097462



Internal ID20664502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169330601..169331600hg38UCSC Ensembl
chr3:169048389..169049388hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366510
Supporting Variants
Samples
Known GenesMECOM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097462
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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