A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077585



Internal ID21986818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123382618..123382618hg38UCSC Ensembl
chr8:124394858..124394858hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381417
hg191417
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586187
Samples
Known GenesATAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077585
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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