A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533557



Internal ID20906918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72745194..72764170hg38UCSC Ensembl
chr17:70741333..70760309hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3818977
hg1918977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037911
Samples
Known GenesSLC39A11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533557
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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