A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882879



Internal ID22657856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7911342..7911397hg38UCSC Ensembl
chr1:7971402..7971457hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388105
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882879
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