A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281637



Internal ID20490855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101623780..101623780hg38UCSC Ensembl
chr8:102636008..102636008hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753613
Supporting Variants
Samples
Known GenesGRHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281637
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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