A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385711



Internal ID21043264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154562692..154563279hg38UCSC Ensembl
chr4:155483844..155484431hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110963
Samples
Known GenesFGB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385711
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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