A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521847



Internal ID20895208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72754057..72773644hg38UCSC Ensembl
chr17:70750196..70769783hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3819588
hg1919588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184542
Samples
Known GenesSLC39A11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521847
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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