A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521333



Internal ID20894694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62971016..63008563hg38UCSC Ensembl
chr17:61048377..61085924hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3837548
hg1937548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188837
Samples
Known GenesMIR548W
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521333
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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