A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921011



Internal ID22696234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:792862..798751hg38UCSC Ensembl
chr7:832499..838388hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg385890
hg195890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442117
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921011
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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