A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145929



Internal ID21447477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22760188..22760188hg38UCSC Ensembl
chr7:22799807..22799807hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639235
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145929
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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