A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576600



Internal ID21768643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154225756..154225756hg38UCSC Ensembl
chr5:153605316..153605316hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080443
Supporting Variants
Samples
Known GenesGALNT10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576600
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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