A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157699



Internal ID21472349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25434979..25434979hg38UCSC Ensembl
chr7:25474598..25474598hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635100
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157699
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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