A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920049



Internal ID22695272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148810706..148810767hg38UCSC Ensembl
chr7:148507798..148507859hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434568
Samples
Known GenesEZH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920049
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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