A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284315



Internal ID20493533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239476551..239476551hg38UCSC Ensembl
chr2:240398245..240398245hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761509
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284315
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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