A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359929



Internal ID21017482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22398619..22399075hg38UCSC Ensembl
chr4:22400242..22400698hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212861
Samples
Known GenesGPR125
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359929
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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