A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505684



Internal ID20878957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17311077..17411265hg38UCSC Ensembl
chr17:17214391..17314579hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38100189
hg19100189
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193017
Samples
Known GenesNT5M
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505684
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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