A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143920



Internal ID21420631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107730128..107730128hg38UCSC Ensembl
chr7:107370573..107370573hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg381611
hg191611
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633155
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143920
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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