A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155134



Internal ID21441889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:206697..206697hg38UCSC Ensembl
chr7:206697..206697hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5636558
Supporting Variants
SamplesHG00732
Known GenesFAM20C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155134
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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