A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101378



Internal ID22010611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6318734..6318734hg38UCSC Ensembl
chr19:6318745..6318745hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622499
Samples
Known GenesACER1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101378
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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