A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332638



Internal ID20865811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:199654401..199656900hg38UCSC Ensembl
chr1:199623529..199626028hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332638
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