A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128586



Internal ID21463549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47467865..47467916hg38UCSC Ensembl
chr4:47469882..47469933hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575277
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128586
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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