A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324281



Internal ID20857406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153096385..153115461hg38UCSC Ensembl
chr1:153068861..153087937hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3819077
hg1919077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200465
Samples
Known GenesSPRR2F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324281
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