A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578731



Internal ID21527203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100607754..100607884hg38UCSC Ensembl
chr4:101528911..101529041hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134672
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578731
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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