A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462034



Internal ID239970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169269309..169270858hg38UCSC Ensembl
chr4:170190460..170192009hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg381550
hg191550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16959129
Samples
Known GenesSH3RF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462034
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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