A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004626



Internal ID21913969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99675597..99675669hg38UCSC Ensembl
chr7:99273220..99273292hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560078
Samples
Known GenesCYP3A5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004626
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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