A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324205



Internal ID20857330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182330045..182350555hg38UCSC Ensembl
chr1:182299180..182319690hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3820511
hg1920511
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324205
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