A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377454



Internal ID21035007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9760743..9945216hg38UCSC Ensembl
chr5:9760855..9945328hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38184474
hg19184474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135739
Samples
Known GenesLOC285692
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377454
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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