A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611152



Internal ID20984223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99694764..99695614hg38UCSC Ensembl
chr7:99292387..99293237hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38851
hg19851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162442
Samples
Known GenesCYP3A7-CYP3AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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