A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519948



Internal ID20893309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5294701..5298000hg38UCSC Ensembl
chr18:5294700..5297999hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177458
Samples
Known GenesZBTB14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519948
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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