A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071976



Internal ID21981209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48663810..48663810hg38UCSC Ensembl
chr8:49576370..49576370hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595797
Samples
Known GenesLOC101929268
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071976
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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