A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070385



Internal ID21979618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74835097..74835097hg38UCSC Ensembl
chr5:74130922..74130922hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544163
Samples
Known GenesFAM169A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070385
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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