A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633128



Internal ID21581433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42474295..42474295hg38UCSC Ensembl
chr5:42474397..42474397hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136129
SamplesHG03125
Known GenesGHR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633128
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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