A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611297



Internal ID21803344
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 StatusS
Merged Variantsnsv6087664
Supporting Variants
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611297
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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