A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603026



Internal ID20976097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122721599..123353768hg38UCSC Ensembl
chr7:122361653..122993822hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38632170
hg19632170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149398
Samples
Known GenesCADPS2, SLC13A1, TAS2R16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603026
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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