A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923672



Internal ID22698899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107857448..107859143hg38UCSC Ensembl
chr7:107497893..107499588hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381696
hg191696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446689
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923672
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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