A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361904



Internal ID21019457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9621107..10087876hg38UCSC Ensembl
chr4:9622731..10089500hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38466770
hg19466770
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5188n223
Supporting Variantsnssv18214354
Samples
Known GenesDRD5, MIR3138, SLC2A9, WDR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361904
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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