A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322975



Internal ID20856090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91023079..91026625hg38UCSC Ensembl
chr1:91488636..91492182hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg383547
hg193547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065105
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322975
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