A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386039



Internal ID21043592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:123856101..123856800hg38UCSC Ensembl
chr4:124777256..124777955hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109737
Samples
Known GenesLINC01091
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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