A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355376



Internal ID21012929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210106087..210107295hg38UCSC Ensembl
chr2:210970811..210972019hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg381209
hg191209
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208124
Samples
Known GenesKANSL1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355376
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