A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331030



Internal ID20864190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91141701..91143300hg38UCSC Ensembl
chr1:91607258..91608857hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331030
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