A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110384



Internal ID22019617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13926000..13926000hg38UCSC Ensembl
chr19:14036813..14036813hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635541
Samples
Known GenesCC2D1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110384
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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