A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145154



Internal ID20712194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71824950..71830277hg38UCSC Ensembl
chr6:72534653..72539980hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg385328
hg195328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412511
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145154
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