A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102872



Internal ID22012107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12973863..12973863hg38UCSC Ensembl
chr19:13084677..13084677hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619346
Samples
Known GenesDAND5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102872
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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