A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102224



Internal ID22011459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29957296..29957296hg38UCSC Ensembl
chr19:30448203..30448203hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632963
Samples
Known GenesURI1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102224
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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