A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552741



Internal ID20925867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31455497..31456379hg38UCSC Ensembl
chr22:31851483..31852365hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38883
hg19883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073731
Samples
Known GenesEIF4ENIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552741
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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