A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284319



Internal ID20493537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:150060150..150061622hg38UCSC Ensembl
chr2:150916664..150918136hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg381473
hg191473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741046
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284319
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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