A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765563



Internal ID20541423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72948276..72948276hg38UCSC Ensembl
chr17:70944415..70944415hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290538
Samples
Known GenesSLC39A11
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765563
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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