A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142562



Internal ID21456868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121480978..121480978hg38UCSC Ensembl
chr7:121121032..121121032hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635533
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142562
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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