A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265013



Internal ID20474231
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 StatusS
Merged Variantsnsv4737773
Supporting Variants
Samples
Known GenesCAPRIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265013
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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