A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107972



Internal ID22017207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8247508..8247508hg38UCSC Ensembl
chrUn_gl000220:146686..146686hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107972
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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