A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155857



Internal ID21465163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99180745..99180745hg38UCSC Ensembl
chr7:98778368..98778368hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632336
Supporting Variants
SamplesHG03065
Known GenesKPNA7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155857
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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