A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096860



Internal ID22006093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61733816..61733816hg38UCSC Ensembl
chr14:62200534..62200534hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605472
Samples
Known GenesHIF1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096860
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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