A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331255



Internal ID20864417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200765449..200770596hg38UCSC Ensembl
chr1:200734577..200739724hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg385148
hg195148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056912
Samples
Known GenesCAMSAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331255
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