A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122004



Internal ID21500363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64273977..64274110hg38UCSC Ensembl
chr4:65139695..65139828hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579755
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122004
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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