A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925705



Internal ID22700932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93622219..93623924hg38UCSC Ensembl
chr7:93251531..93253236hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381706
hg191706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925705
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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