A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327900



Internal ID20861044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:176365802..176372781hg38UCSC Ensembl
chr1:176334938..176341917hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg386980
hg196980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327900
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