A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343156



Internal ID21000709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32276255..32293243hg38UCSC Ensembl
chr2:32501324..32518312hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3816989
hg1916989
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208203
Samples
Known GenesYIPF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343156
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