A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897864



Internal ID22672973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73270595..73270672hg38UCSC Ensembl
chr5:72566422..72566499hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897864
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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