A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737773



Internal ID20513736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30720728..30720795hg38UCSC Ensembl
chr12:30873662..30873729hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265013
Samples
Known GenesCAPRIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737773
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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