A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747314



Internal ID20523332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61447825..61452435hg38UCSC Ensembl
chr2:61674960..61679570hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg384611
hg194611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295690
Samples
Known GenesUSP34
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747314
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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