A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135689



Internal ID21473789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138837613..138837733hg38UCSC Ensembl
chr4:139758767..139758887hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582978
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135689
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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