A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329538



Internal ID20862690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17704295..17708593hg38UCSC Ensembl
chr1:18030790..18035088hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg384299
hg194299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053775
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329538
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