A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916847



Internal ID22692066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169692358..169693261hg38UCSC Ensembl
chr6:170092454..170093357hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38904
hg19904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425307
Samples
Known GenesWDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916847
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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