A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432114



Internal ID21089667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148875546..148882141hg38UCSC Ensembl
chr7:148572638..148579233hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386596
hg196596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153980
Samples
Known GenesEZH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432114
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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