A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906174



Internal ID22681370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:169810574..169810650hg38UCSC Ensembl
chr2:170667084..170667160hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390750
Samples
Known GenesSSB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906174
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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