A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278955



Internal ID20488173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74024994..74025117hg38UCSC Ensembl
chr2:74252121..74252244hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731683
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278955
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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