A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267921



Internal ID20477139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68978217..68978217hg38UCSC Ensembl
chr2:69205349..69205349hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751632
Supporting Variants
Samples
Known GenesGKN1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267921
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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