A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431987



Internal ID22489858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91888868..91889019hg38UCSC Ensembl
chr7:91518182..91518333hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921942
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431987
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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