A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283191



Internal ID20492409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238783397..238783397hg38UCSC Ensembl
chr2:239692038..239692038hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752864
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283191
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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