A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096929



Internal ID21484151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41670760..41670760hg38UCSC Ensembl
chr17:39827012..39827012hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg382038
hg192038
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660183
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096929
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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