A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134061



Internal ID21416363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169178281..169178332hg38UCSC Ensembl
chr4:170099432..170099483hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574677
Supporting Variants
SamplesHG00731
Known GenesSH3RF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134061
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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