A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039213



Internal ID20606253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81881369..81882428hg38UCSC Ensembl
chr17:79839245..79840304hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381060
hg191060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530043
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039213
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