A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028289



Internal ID21937632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1643243..1643301hg38UCSC Ensembl
chr17:1546537..1546595hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635843
Samples
Known GenesSCARF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028289
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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