A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448692



Internal ID22506562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65863474..65864542hg38UCSC Ensembl
chr8:66775709..66776777hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg381069
hg191069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5913986
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448692
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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