A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295552



Internal ID20504770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19586053..19586456hg38UCSC Ensembl
chr6:19586284..19586687hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745601
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295552
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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