A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448546



Internal ID22506416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42765756..42766209hg38UCSC Ensembl
chr8:42620899..42621352hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38454
hg19454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916988
Supporting Variants
Samples
Known GenesCHRNA6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448546
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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