A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919804



Internal ID22695026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27255733..27257647hg38UCSC Ensembl
chr7:27295352..27297266hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg381915
hg191915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443770
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919804
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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