A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514358



Internal ID20887711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5126158..5135104hg38UCSC Ensembl
chr17:5029453..5038399hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg388947
hg198947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036847
Samples
Known GenesUSP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514358
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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