A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141861



Internal ID20708901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149267972..149285693hg38UCSC Ensembl
chr6:149589108..149606829hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3817722
hg1917722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616957
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141861
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