A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393258



Internal ID21050811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154563941..154564324hg38UCSC Ensembl
chr4:155485093..155485476hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110964
Samples
Known GenesFGB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393258
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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