A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326676



Internal ID20859813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25697956..25703898hg38UCSC Ensembl
chr1:26024447..26030389hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385943
hg195943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060550
Samples
Known GenesMAN1C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326676
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