A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134055



Internal ID21410289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169178281..169178281hg38UCSC Ensembl
chr4:170099432..170099432hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632627
Supporting Variants
SamplesHG00512
Known GenesSH3RF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134055
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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