A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387866



Internal ID21045419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147538037..147970462hg38UCSC Ensembl
chr4:148459189..148891613hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg38432426
hg19432425
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212037
Samples
Known GenesARHGAP10, EDNRA, MIR4799, PRMT10, TMEM184C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387866
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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