A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367466



Internal ID21025019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22490067..22504440hg38UCSC Ensembl
chr4:22491690..22506063hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3814374
hg1914374
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212862
Samples
Known GenesGPR125
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367466
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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