A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898978



Internal ID22674103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42770662..42770927hg38UCSC Ensembl
chr6:42738400..42738665hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898978
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