A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632627



Internal ID21580932
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 StatusM
Merged Variants
Supporting Variantsnssv17128906, nssv17134055
SamplesHG00512, HG00731
Known GenesSH3RF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632627
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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