A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637327



Internal ID21585632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176885574..176885574hg38UCSC Ensembl
chr5:176312575..176312575hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123053
SamplesHG03732
Known GenesHK3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637327
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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