A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270888



Internal ID20480106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206864625..206864625hg38UCSC Ensembl
chr1:207037970..207037970hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751519
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270888
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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