A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514380



Internal ID20887733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6909801..6971700hg38UCSC Ensembl
chr17:6813120..6875019hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3861900
hg1961900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037590
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514380
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