A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5471092



Internal ID248836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122380606..122380682hg38UCSC Ensembl
chr4:123301761..123301837hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16955178
Samples
Known GenesADAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5471092
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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