A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512016



Internal ID20885346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39220850..39228787hg38UCSC Ensembl
chr17:37377103..37385040hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg387938
hg197938
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184578
Samples
Known GenesSTAC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512016
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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