A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285448



Internal ID20494666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56158413..56158413hg38UCSC Ensembl
chr1:56624085..56624085hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766961
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285448
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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