A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096438



Internal ID22005671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14487429..14487429hg38UCSC Ensembl
chr10:14529428..14529428hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583453
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096438
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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