A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002362



Internal ID21911705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96835783..96851069hg38UCSC Ensembl
chr5:96171486..96186772hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3815287
hg1915287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548612
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002362
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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