A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151653



Internal ID21405253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90315095..90315095hg38UCSC Ensembl
chr7:89944409..89944409hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg386078
hg196078
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630424
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151653
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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