A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063101



Internal ID21972334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101509187..101509187hg38UCSC Ensembl
chr8:102521415..102521415hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589460
Samples
Known GenesGRHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063101
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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