A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376061



Internal ID21033614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146117442..146223508hg38UCSC Ensembl
chr4:147038594..147144660hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg38106067
hg19106067
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212024
Samples
Known GenesLINC01095, LSM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376061
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