A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400739



Internal ID21058292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73452267..73712273hg38UCSC Ensembl
chr6:74161990..74421996hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38260007
hg19260007
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225097
Samples
Known GenesCD109, EEF1A1, MB21D1, MTO1, SLC17A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400739
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