A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431707



Internal ID22489577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11210317..11210373hg38UCSC Ensembl
chr8:11067826..11067882hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908305
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431707
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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