A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455427



Internal ID21112980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73368135..73377416hg38UCSC Ensembl
chr10:75127893..75137174hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg389282
hg199282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178426
Samples
Known GenesANXA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455427
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