A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000209



Internal ID21909552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57374723..57374774hg38UCSC Ensembl
chr5:56670550..56670601hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000209
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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