A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395909



Internal ID22453779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10875801..10876098hg38UCSC Ensembl
chr2:11015927..11016224hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874756
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395909
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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