A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761380



Internal ID20537240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42576060..42576060hg38UCSC Ensembl
chr5:42576162..42576162hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265455
Samples
Known GenesGHR
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761380
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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