A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142581



Internal ID21460791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90613805..90613805hg38UCSC Ensembl
chr6:91323524..91323524hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642533
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142581
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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