A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628693



Internal ID21576998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163587803..163587803hg38UCSC Ensembl
chr4:164508955..164508955hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119925
SamplesHG03486
Known GenesMARCH1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628693
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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