A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600184



Internal ID20973255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147531464..147544997hg38UCSC Ensembl
chr6:147852600..147866133hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3813534
hg1913534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141170
Samples
Known GenesSAMD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600184
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