A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414992



Internal ID22472862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36670230..36677916hg38UCSC Ensembl
chr3:36711721..36719407hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg387687
hg197687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894747
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414992
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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