A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747886



Internal ID20523908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10756064..10756401hg38UCSC Ensembl
chr5:10756176..10756513hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279281
Samples
Known GenesDAP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747886
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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