A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887771



Internal ID22662767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77008573..77008631hg38UCSC Ensembl
chr5:76304398..76304456hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887771
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