A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501768



Internal ID20875005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28649636..28650616hg38UCSC Ensembl
chr17:26976654..26977634hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38981
hg19981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035194
Samples
Known GenesSDF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501768
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