A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362592



Internal ID21020145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21353189..21398838hg38UCSC Ensembl
chr4:21354812..21400461hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3845650
hg1945650
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212856
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362592
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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