A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079778



Internal ID21989011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75612323..75612323hg38UCSC Ensembl
chr5:74908148..74908148hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556209
Samples
Known GenesANKDD1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079778
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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