A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603272



Internal ID20976343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99671730..99679256hg38UCSC Ensembl
chr7:99269353..99276879hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg387527
hg197527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162440
Samples
Known GenesCYP3A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603272
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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