A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141559



Internal ID21470786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68395321..68395321hg38UCSC Ensembl
chr7:67860308..67860308hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5638153
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141559
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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