A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157316



Internal ID21489663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50426423..50426423hg38UCSC Ensembl
chr6:50394136..50394136hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630106
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157316
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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