A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146799



Internal ID21456966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71723743..71723743hg38UCSC Ensembl
chr6:72433446..72433446hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630635
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146799
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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