A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157269



Internal ID21451518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60287073..60287073hg38UCSC Ensembl
chr8:61199632..61199632hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3817595
hg1917595
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642429
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157269
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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