A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908618



Internal ID22683828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130701910..130703861hg38UCSC Ensembl
chr7:130386739..130388690hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg381952
hg191952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908618
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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