A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148113



Internal ID21467952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99063215..99063285hg38UCSC Ensembl
chr7:98660838..98660908hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576717
Supporting Variants
SamplesHG03125
Known GenesSMURF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148113
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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