A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389195



Internal ID21046748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120084501..120086100hg38UCSC Ensembl
chr4:121005656..121007255hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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