A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437806



Internal ID22495676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29175557..29188366hg38UCSC Ensembl
chr9:29175555..29188364hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3812810
hg1912810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912027
Supporting Variants
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437806
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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