A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356685



Internal ID21014238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9575444..10681382hg38UCSC Ensembl
chr4:9577068..10683006hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381105939
hg191105939
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5184n223
Supporting Variantsnssv18214343
Samples
Known GenesCLNK, DRD5, MIR3138, SLC2A9, WDR1, ZNF518B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356685
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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