A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142929



Internal ID21477478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121474423..121479199hg38UCSC Ensembl
chr6:121795569..121800345hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384777
hg194777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566743
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142929
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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