A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330147



Internal ID20863301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150519009..150527802hg38UCSC Ensembl
chr1:150491485..150500278hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg388794
hg198794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330147
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