A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356540



Internal ID21014093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9969888..10322041hg38UCSC Ensembl
chr4:9971512..10323665hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38352154
hg19352154
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214418
Samples
Known GenesMIR3138, SLC2A9, WDR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356540
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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