A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001710



Internal ID21911053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151454105..151454710hg38UCSC Ensembl
chr5:150833666..150834271hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567759
Samples
Known GenesSLC36A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001710
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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