A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641688



Internal ID21589993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96896864..96896864hg38UCSC Ensembl
chr5:96232568..96232568hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140275
SamplesHG00513
Known GenesERAP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641688
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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