A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150416



Internal ID21457037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21248154..21248154hg38UCSC Ensembl
chr7:21287773..21287773hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5638191
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150416
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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