A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103491



Internal ID22012724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33218661..33218661hg38UCSC Ensembl
chr19:33709567..33709567hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635285
Samples
Known GenesSLC7A10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103491
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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