A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921596



Internal ID22696820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19230358..19231491hg38UCSC Ensembl
chr7:19269981..19271114hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg381134
hg191134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921596
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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