A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100672



Internal ID22009905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51357375..51357375hg38UCSC Ensembl
chr19:51860629..51860629hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637353
Samples
Known GenesETFB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100672
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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