A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326095



Internal ID20859229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47157144..47170011hg38UCSC Ensembl
chr1:47622816..47635683hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3812868
hg1912868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326095
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