A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497867



Internal ID20871075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43871214..43889596hg38UCSC Ensembl
chr17:41948582..41966964hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3818383
hg1918383
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184775
Samples
Known GenesMPP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497867
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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