A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005491



Internal ID21914834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177451791..177451845hg38UCSC Ensembl
chr5:176878792..176878846hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570474
Samples
Known GenesPRR7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005491
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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