A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519005



Internal ID20892366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51292850..51678463hg38UCSC Ensembl
chr17:49370211..49755823hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38385614
hg19385613
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181593
Samples
Known GenesCA10, UTP18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519005
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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