A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367170



Internal ID21024723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21412807..21506981hg38UCSC Ensembl
chr4:21414430..21508604hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3894175
hg1994175
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212859
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367170
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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