A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17405169



Internal ID22463039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88860917..89176323hg38UCSC Ensembl
chr2:89160429..89475807hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38315407
hg19315379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17405169
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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