A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150556



Internal ID21506318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88187635..88187635hg38UCSC Ensembl
chr6:88897354..88897354hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640225
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150556
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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