A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635634



Internal ID21583939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83531853..83531853hg38UCSC Ensembl
chr5:82827672..82827672hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145292
SamplesHG03125
Known GenesVCAN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635634
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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