A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413953



Internal ID21071506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94607253..94614164hg38UCSC Ensembl
chr5:93942958..93949869hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg386912
hg196912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136469
Samples
Known GenesKIAA0825
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413953
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer