A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732207



Internal ID20508130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49489800..49489861hg38UCSC Ensembl
chr15:49781997..49782058hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267942
Samples
Known GenesFAM227B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732207
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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