A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356312



Internal ID21013865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25238869..25254793hg38UCSC Ensembl
chr4:25240491..25256415hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3815925
hg1915925
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211798
Samples
Known GenesPI4K2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356312
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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