A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129718



Internal ID21474301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165843450..165843450hg38UCSC Ensembl
chr4:166764602..166764602hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg386077
hg196077
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626812
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129718
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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