A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739727



Internal ID20515702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6846089..6846152hg38UCSC Ensembl
chr5:6846202..6846265hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289707
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739727
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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