A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914983



Internal ID22690201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101092520..101092606hg38UCSC Ensembl
chr7:100735801..100735887hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433238
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914983
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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