A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400152



Internal ID21057705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78032925..78033311hg38UCSC Ensembl
chr5:77328749..77329135hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135158
Samples
Known GenesAP3B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400152
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