A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133034



Internal ID21498047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138739251..138739370hg38UCSC Ensembl
chr4:139660405..139660524hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575913
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133034
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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