A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124442



Internal ID21501351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40633734..40635312hg38UCSC Ensembl
chr4:40635751..40637329hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381579
hg191579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5564962
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124442
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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