A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072785



Internal ID21982018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:138206769..138206769hg38UCSC Ensembl
chr8:139219012..139219012hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593912
Samples
Known GenesFAM135B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072785
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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