A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087664



Internal ID21996897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71768959..71768959hg38UCSC Ensembl
chr15:72061298..72061298hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611297
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087664
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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