A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084430



Internal ID21486135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70361257..70361257hg38UCSC Ensembl
chr17:68357398..68357398hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg386038
hg196038
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662576
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084430
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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