A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153519



Internal ID21451965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61762543..61762543hg38UCSC Ensembl
chr8:62675102..62675102hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630001
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153519
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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