A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153807



Internal ID21406811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43004552..43004552hg38UCSC Ensembl
chr7:43044151..43044151hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628408
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153807
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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