A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761307



Internal ID20537167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118969988..118969988hg38UCSC Ensembl
chr6:119291153..119291153hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277401
Samples
Known GenesFAM184A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761307
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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