A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412132



Internal ID21069685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37100097..37127760hg38UCSC Ensembl
chr6:37067873..37095536hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3827664
hg1927664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236618
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412132
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