A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753613



Internal ID20529473
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 StatusM
Merged Variants
Supporting Variantsnssv16281637
Samples
Known GenesGRHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753613
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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