A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900931



Internal ID22676078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169229924..169230058hg38UCSC Ensembl
chr4:170151075..170151209hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418136
Samples
Known GenesSH3RF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900931
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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