A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102037



Internal ID22011270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18377415..18377415hg38UCSC Ensembl
chr19:18488225..18488225hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg382549
hg192549
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102037
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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