A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575506



Internal ID21523935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15791367..15791443hg38UCSC Ensembl
chr4:15792990..15793066hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137153
SamplesNA18939
Known GenesCD38
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575506
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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