A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277761



Internal ID20486979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244263419..244263419hg38UCSC Ensembl
chr1:244426721..244426721hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763164
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277761
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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