A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143199



Internal ID21409340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99180747..99180816hg38UCSC Ensembl
chr7:98778370..98778439hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568824
Supporting Variants
SamplesHG00512
Known GenesKPNA7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143199
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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