A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153960



Internal ID21425037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16655..16655hg38UCSC Ensembl
chr7:16655..16655hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635485
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153960
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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