A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043972



Internal ID20611012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74921076..74921733hg38UCSC Ensembl
chr18:72633032..72633689hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530044
Supporting Variants
Samples
Known GenesZNF407
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00088


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