A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387068



Internal ID21044621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:90345502..90381422hg38UCSC Ensembl
chr4:91266653..91302573hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3835921
hg1935921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215243
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387068
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