A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000360



Internal ID21909703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57031043..57031241hg38UCSC Ensembl
chr5:56326870..56327068hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000360
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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