A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104821



Internal ID22014054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38328889..38328889hg38UCSC Ensembl
chr19:38819529..38819529hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626567
Samples
Known GenesKCNK6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104821
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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