A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153928



Internal ID21442680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139002765..139002765hg38UCSC Ensembl
chr6:139323902..139323902hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628173
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153928
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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