A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108004



Internal ID22017239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57540925..57540925hg38UCSC Ensembl
chr19:58052293..58052293hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382201
hg192201
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108004
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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