A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392180



Internal ID21049733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121561283..121567753hg38UCSC Ensembl
chr4:122482438..122488908hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg386471
hg196471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108992
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392180
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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