A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877081



Internal ID22652044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96389496..96390927hg38UCSC Ensembl
chr1:96855052..96856483hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381432
hg191432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877081
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