A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276302



Internal ID20485520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71374992..71374992hg38UCSC Ensembl
chr6:72084695..72084695hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754142
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276302
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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