A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17405992



Internal ID22463862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10448..10783hg38UCSC Ensembl
chr2:10448..10783hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881703
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17405992
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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