A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15203123



Internal ID21341933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99675638..99675638hg38UCSC Ensembl
chr7:99273261..99273261hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3925435
Supporting Variants
SamplesHG002
Known GenesCYP3A5
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15203123
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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