A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501597



Internal ID20874833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31858301..31859400hg38UCSC Ensembl
chr17:30185320..30186419hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034915
Samples
Known GenesCOPRS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501597
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