A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140723



Internal ID21419268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165749182..165749182hg38UCSC Ensembl
chr6:166162670..166162670hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5629105
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140723
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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