A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327602



Internal ID20860742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149562801..149566500hg38UCSC Ensembl
chr1:148764738..148788781hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg383700
hg1924044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201496
Samples
Known GenesLOC101929780
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327602
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer