A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088452



Internal ID21997685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73204877..73204877hg38UCSC Ensembl
chr10:74964635..74964635hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579714
Samples
Known GenesFAM149B1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088452
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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