A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035993



Internal ID21945336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13879941..13880054hg38UCSC Ensembl
chr17:13783258..13783371hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618566
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035993
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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