A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575973



Internal ID21524407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:74777989..74778069hg38UCSC Ensembl
chr4:75703199..75703279hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124945
SamplesHG03486
Known GenesBTC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575973
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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