A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434408



Internal ID22492278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96061286..96061286hg38UCSC Ensembl
chr6:96509162..96509162hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5960872
Supporting Variants
Samples
Known GenesFUT9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434408
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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