A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106163



Internal ID20673203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101644094..101649574hg38UCSC Ensembl
chr4:102565251..102570731hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg385481
hg195481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106163
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