A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260698



Internal ID20469916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95046823..95046896hg38UCSC Ensembl
chr2:95712568..95712641hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733840
Supporting Variants
Samples
Known GenesMAL
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260698
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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