A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138759



Internal ID21402345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36492031..36492031hg38UCSC Ensembl
chr3:36533523..36533523hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613493
Supporting Variants
SamplesHG00171
Known GenesSTAC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138759
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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