A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035195



Internal ID20602235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28692261..28692938hg38UCSC Ensembl
chr17:27019279..27019956hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498817
Supporting Variants
Samples
Known GenesSUPT6H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.09428


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