A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615286



Internal ID20988357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122942257..123142187hg38UCSC Ensembl
chr7:122582311..122782241hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38199931
hg19199931
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223671
Samples
Known GenesSLC13A1, TAS2R16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615286
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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