A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441883



Internal ID22499753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47427825..47634746hg38UCSC Ensembl
chr8:48340387..48547308hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38206922
hg19206922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5913634
Supporting Variants
Samples
Known GenesSPIDR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441883
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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