A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574393



Internal ID21766436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158169402..158169402hg38UCSC Ensembl
chr6:158590434..158590434hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076806
Supporting Variants
Samples
Known GenesGTF2H5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574393
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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