A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157571



Internal ID21485435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35203776..35203776hg38UCSC Ensembl
chr7:35243388..35243388hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg381725
hg191725
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640988
Supporting Variants
SamplesNA12878
Known GenesTBX20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157571
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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