A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635866



Internal ID21584171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72595309..72595309hg38UCSC Ensembl
chr5:71891136..71891136hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153340
SamplesHG00864
Known GenesLOC102477328
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635866
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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