A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625163



Internal ID21573468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185290718..185290718hg38UCSC Ensembl
chr4:186211872..186211872hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133803
SamplesHG03683
Known GenesSNX25
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625163
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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