A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768176



Internal ID20544036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50609990..50609990hg38UCSC Ensembl
chr20:49226527..49226527hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271190
Samples
Known GenesFAM65C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768176
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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